Publications by authors named "Angela M Kaindl"

85Publications

Intravenous Nimodipine Treatment for Severe Episode of ATP1A2 Hemiplegic Migraine.

Pediatr Neurol 2020 Jul 22;112:71-72. Epub 2020 Jul 22.

Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany; Center for Chronically Sick Children, Charité - Universitätsmedizin Berlin, Berlin, Germany; Institute for Cell Biology and Neurobiology, Charité - Universitätsmedizin Berlin, Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.pediatrneurol.2020.07.009DOI Listing
July 2020

Clinical Outcome of Children With Corpus Callosum Agenesis.

Pediatr Neurol 2020 Aug 11;112:47-52. Epub 2020 Aug 11.

Center for Chronically Sick Children, Charité - Universitätsmedizin Berlin, Berlin, Germany; Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany; Institute of Cell Biology and Neurobiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

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http://dx.doi.org/10.1016/j.pediatrneurol.2020.07.013DOI Listing
August 2020

Presence of anti-neuronal antibodies in children with neurological disorders beyond encephalitis.

Eur J Paediatr Neurol 2020 Jul 30. Epub 2020 Jul 30.

Department of Pediatric Neurology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität, Humboldt-Universität, Berlin Institute of Health, Berlin, Germany; Center for Chronically Sick Children, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität, Humboldt-Universität, Berlin Institute of Health, Berlin, Germany; NeuroCure Clinical Research Center, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität, Humboldt-Universität, Berlin Institute of Health, Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2020.07.004DOI Listing
July 2020

The clinical-phenotype continuum in DYNC1H1-related disorders-genomic profiling and proposal for a novel classification.

J Hum Genet 2020 Aug 12. Epub 2020 Aug 12.

Department of Pediatrics, Faculty of Medicine and University Hospital Cologne, Center for Molecular Medicine Cologne (CMMC), Center for Rare Diseases, University of Cologne, Cologne, Germany.

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http://dx.doi.org/10.1038/s10038-020-0803-1DOI Listing
August 2020

Age-specific occurrence of pathological fractures in patients with spina bifida.

Eur J Pediatr 2020 May 6;179(5):773-779. Epub 2020 Jan 6.

Charité-Universitätsmedizin Berlin, Center for Chronically Sick Children, Berlin, Germany.

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http://dx.doi.org/10.1007/s00431-019-03537-yDOI Listing
May 2020

MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis.

Brain 2020 01;143(1):55-68

Laboratory of Embryology and Genetics of Human Malformation, Institut National de la Santé et de la Recherche Médicale (INSERM) UMR 1163, Institut Imagine, Paris, France.

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http://dx.doi.org/10.1093/brain/awz379DOI Listing
January 2020

Early Onset, Long Illness Duration, Epilepsy Type, and Polypharmacy Have an Adverse Effect on Psychosocial Outcome in Children with Epilepsy.

Neuropediatrics 2020 04 21;51(2):164-169. Epub 2019 Nov 21.

Charité - Universitätsmedizin Berlin, Center for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Berlin, Germany.

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http://dx.doi.org/10.1055/s-0039-3399529DOI Listing
April 2020

Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family-The Role of Next Generation Sequencing in Neuromuscular Disorders.

Neuropediatrics 2020 02 18;51(1):72-75. Epub 2019 Oct 18.

Charité-Universitätsmedizin Berlin, Klinik für Pädiatrie mit Schwerpunkt Neurologie, Augustenburger Platz 1, Berlin, Germany.

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http://dx.doi.org/10.1055/s-0039-1695787DOI Listing
February 2020

Congenital microcephaly-linked CDK5RAP2 affects eye development.

Ann Hum Genet 2020 01 29;84(1):87-91. Epub 2019 Jul 29.

Institute of Cell and Neurobiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

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http://dx.doi.org/10.1111/ahg.12343DOI Listing
January 2020

Fulminant cerebral venous thrombosis associated with the m.3243A>G MELAS mutation: A new guise for an old disease.

Brain Dev 2019 Nov 22;41(10):901-904. Epub 2019 Jul 22.

Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health (BIH), Department of Neuropediatrics, Berlin, Germany; Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health (BIH), Sozialpädiatrisches Zentrum, Berlin, Germany; Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health (BIH), NeuroCure Clinical Research Center, Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.braindev.2019.07.002DOI Listing
November 2019

Altered inhibition and excitation in neocortical circuits in congenital microcephaly.

Neurobiol Dis 2019 09 15;129:130-143. Epub 2019 May 15.

Charité - Universitätsmedizin Berlin, Institute of Cell- and Neurobiology, Charitéplatz 1, 10117 Berlin, Germany; Charité - Universitätsmedizin Berlin, Center for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Augustenburger Platz 1, 13353 Berlin, Germany; Charité - Universitätsmedizin Berlin, Department of Pediatric Neurology, Augustenburger Platz 1, 13353 Berlin, Germany; Berlin Institute of Health (BIH), Anna-Louisa-Karsch Strasse 2, 10178 Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.nbd.2019.05.008DOI Listing
September 2019

Subtelomeric methylation distinguishes between subtypes of Immunodeficiency, Centromeric instability and Facial anomalies syndrome.

Hum Mol Genet 2018 10;27(20):3568-3581

Molecular Medicine Laboratory, Rambam Health Care Campus and Rappaport Faculty of Medicine, Technion, Haifa, Israel.

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https://academic.oup.com/hmg/article/27/20/3568/5054136
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http://dx.doi.org/10.1093/hmg/ddy265DOI Listing
October 2018

Identification of a novel homozygous TRAPPC9 gene mutation causing non-syndromic intellectual disability, speech disorder, and secondary microcephaly.

Am J Med Genet B Neuropsychiatr Genet 2017 Dec 14;174(8):839-845. Epub 2017 Oct 14.

Charité - Universitätsmedizin Berlin, Institute of Neuroanatomy and Cell Biology, Berlin, Germany.

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http://dx.doi.org/10.1002/ajmg.b.32602DOI Listing
December 2017

Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasia.

Mitochondrion 2017 11 4;37:46-54. Epub 2017 Jul 4.

NeuroCure Clinical Research Center (NCRC), Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Germany; Department of Neuropediatrics, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Germany. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S15677249163028
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http://dx.doi.org/10.1016/j.mito.2017.06.007DOI Listing
November 2017

Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Nat Genet 2017 05;49(6):969

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http://dx.doi.org/10.1038/ng0617-969cDOI Listing
May 2017

Autosomal Recessive Primary Microcephaly (MCPH): An Update.

Neuropediatrics 2017 Jun 11;48(3):135-142. Epub 2017 Apr 11.

Institute of Cell Biology and Neurobiology, Charité - Universitätsmedizin Berlin, Campus Mitte, Berlin, Germany.

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http://dx.doi.org/10.1055/s-0037-1601448DOI Listing
June 2017

Lacosamide Lowers Valproate and Levetiracetam Levels.

Neuropediatrics 2017 Jun 21;48(3):188-189. Epub 2017 Mar 21.

Department of Pediatric Neurology, Center for Chronically Sick Children, Charité University Medicine Berlin, Berlin, Germany.

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http://www.thieme-connect.de/DOI/DOI?10.1055/s-0037-1600112
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http://dx.doi.org/10.1055/s-0037-1600112DOI Listing
June 2017

Pontine Tegmental Cap Dysplasia in an Extremely Preterm Infant and Review of the Literature.

J Child Neurol 2017 03 20;32(3):334-340. Epub 2016 Dec 20.

2 Institute of Cell Biology and Neurobiology, Charité-Universitätsmedizin Berlin, Berlin, Germany.

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http://dx.doi.org/10.1177/0883073816680748DOI Listing
March 2017

CDK5RAP2 Is Required to Maintain the Germ Cell Pool during Embryonic Development.

Stem Cell Reports 2017 02 2;8(2):198-204. Epub 2017 Feb 2.

Institute of Cell Biology and Neurobiology, Charité - Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany; Center for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Charité - Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany; Berlin Institute of Health (BIH), Kapelle-Ufer 2, 10117 Berlin, Germany. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S22136711173001
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http://dx.doi.org/10.1016/j.stemcr.2017.01.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312265PMC
February 2017

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Nat Genet 2017 Feb 9;49(2):238-248. Epub 2017 Jan 9.

Molecular Neurogenetics Unit and Psychiatric and Neurodevelopmental Genetics Unit, Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, USA.

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http://dx.doi.org/10.1038/ng.3743DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473428PMC
February 2017

Phenotype variability of infantile-onset multisystem neurologic, endocrine, and pancreatic disease IMNEPD.

Orphanet J Rare Dis 2016 04 29;11(1):52. Epub 2016 Apr 29.

Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany.

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http://ojrd.biomedcentral.com/articles/10.1186/s13023-016-04
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http://dx.doi.org/10.1186/s13023-016-0433-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850685PMC
April 2016

Golgi-Cox Staining Step by Step.

Front Neuroanat 2016 31;10:38. Epub 2016 Mar 31.

Institute of Cell Biology and Neurobiology, Charité - Universitätsmedizin BerlinBerlin, Germany; Center for Chronically Sick Children (Sozialpädiatrisches Zentrum, SPZ), Charité - Universitätsmedizin BerlinBerlin, Germany.

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http://dx.doi.org/10.3389/fnana.2016.00038DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4814522PMC
April 2016

Acute Disseminated Encephalomyelitis After Human Parechovirus Infection.

Pediatr Infect Dis J 2016 Jan;35(1):35-8

From the *Department of Pediatrics, Charité University Medical Center; †Medical Bioinformatics Group, Free University; ‡Institute for Cell and Neurobiology, Charité University Medical Center; §Center for Social Pediatrics (SPZ), Charité University Medical Center; and ¶National Reference Center for Poliomyelitis and Enteroviruses, Robert Koch Institute, Berlin, Germany.

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http://dx.doi.org/10.1097/INF.0000000000000928DOI Listing
January 2016

Genetic causes of MCPH in consanguineous Pakistani families.

Clin Genet 2016 06 8;89(6):744-5. Epub 2015 Nov 8.

Institute of Cell Biology and Neurobiology, University of Azad Jammu and Kashmir, Muzaffarabad, Pakistan.

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http://dx.doi.org/10.1111/cge.12685DOI Listing
June 2016

Novel Alternative Splice Variants of Mouse Cdk5rap2.

PLoS One 2015 31;10(8):e0136684. Epub 2015 Aug 31.

Institute of Cell Biology and Neurobiology, Charité -Universitätsmedizin Berlin, Berlin, Germany; Department of Pediatric Neurology, Charité -Universitätsmedizin Berlin, Berlin, Germany; Sozialpädiatrisches Zentrum (SPZ), Charité -Universitätsmedizin Berlin, Berlin, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0136684PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4556188PMC
June 2016

What next-generation sequencing (NGS) technology has enabled us to learn about primary autosomal recessive microcephaly (MCPH).

Mol Cell Probes 2015 Oct 4;29(5):271-81. Epub 2015 Jun 4.

Department of Pediatric Neurology, Charité University Medicine, Berlin, Germany; Institute of Cell Biology and Neurobiology, Charité University Medicine, Berlin, Germany.

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http://dx.doi.org/10.1016/j.mcp.2015.05.015DOI Listing
October 2015

Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytes.

Cell Cycle 2015 ;14(13):2044-57

a Institute of Cell Biology and Neurobiology; Charité - Universitätsmedizin Berlin; Campus Mitte ; Berlin , Germany.

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http://dx.doi.org/10.1080/15384101.2015.1044169DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4613649PMC
April 2016

Synaptic NMDA receptor activity is coupled to the transcriptional control of the glutathione system.

Nat Commun 2015 Apr 9;6:6761. Epub 2015 Apr 9.

Centre for Integrative Physiology, University of Edinburgh School of Biomedical Sciences, Hugh Robson Building, George Square, Edinburgh EH8 9XD, UK.

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http://dx.doi.org/10.1038/ncomms7761DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403319PMC
April 2015

Is microcephaly a so-far unrecognized feature of XYY syndrome?

Meta Gene 2014 Dec 31;2:160-3. Epub 2014 Jan 31.

Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353 Berlin, Germany ; SPZ Pediatric Neurology, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353 Berlin, Germany ; Institute of Neuroanatomy and Cell Biology, Charité - Universitätsmedizin Berlin, Campus Mitte, Charitéplatz 1, 10115 Berlin, Germany.

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http://dx.doi.org/10.1016/j.mgene.2013.10.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287790PMC
December 2014

Interstitial 12p deletion involving more than 40 genes in a patient with postnatal microcephaly, psychomotor delay, optic nerve atrophy, and facial dysmorphism.

Meta Gene 2014 Dec 11;2:72-82. Epub 2014 Jan 11.

Department of Pediatric Neurology, Charité-Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353 Berlin, Germany ; SPZ Pediatric Neurology, Charité-Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353 Berlin, Germany ; Institute of Neuroanatomy and Cell Biology, Charité-Universitätsmedizin Berlin, Campus Mitte, Charitéplatz 1, 10115 Berlin, Germany.

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https://linkinghub.elsevier.com/retrieve/pii/S22145400130002
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http://dx.doi.org/10.1016/j.mgene.2013.10.014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4287802PMC
December 2014

Autosomal recessive primary microcephalies (MCPH).

Authors:
Angela M Kaindl

Eur J Paediatr Neurol 2014 Jul 16;18(4):547-8. Epub 2014 Apr 16.

Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Germany; Institute of Cell Biology and Neurobiology, Charité - Universitätsmedizin Berlin, Germany. Electronic address:

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http://www.scientific-journals.co.uk/web_documents/2020103_m
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http://link.springer.com/content/pdf/10.1186%2F1750-1172-6-3
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http://eprints.whiterose.ac.uk/249/1/woodscg3.pdf
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http://linkinghub.elsevier.com/retrieve/pii/S109037981400050
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http://dx.doi.org/10.1016/j.ejpn.2014.03.010DOI Listing
July 2014

Previously reported new type of autosomal recessive primary microcephaly is caused by compound heterozygous ASPM gene mutations.

Cell Cycle 2014 1;13(10):1650-1. Epub 2014 Apr 1.

Department of Pediatric Neurology; Charité University Medicine Berlin; Berlin, Germany; Institute of Cell Biology and Neurobiology; Charité University Medicine Berlin; Berlin, Germany.

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http://dx.doi.org/10.4161/cc.28706DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4050170PMC
February 2016

Diagnostic approach to microcephaly in childhood: a two-center study and review of the literature.

Dev Med Child Neurol 2014 Aug 12;56(8):732-41. Epub 2014 Mar 12.

Abteilung Neuropaediatrie, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.

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http://dx.doi.org/10.1111/dmcn.12425DOI Listing
August 2014

Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation.

Orphanet J Rare Dis 2013 Nov 14;8:178. Epub 2013 Nov 14.

Institute of Cell Biology and Neurobiology, Charité University Medicine Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, Berlin 13353, Germany.

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http://dx.doi.org/10.1186/1750-1172-8-178DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225825PMC
November 2013

Growth and psychomotor development of patients with Duchenne muscular dystrophy.

Eur J Paediatr Neurol 2014 Jan 25;18(1):38-44. Epub 2013 Sep 25.

Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353 Berlin, Germany; SPZ Pediatric Neurology, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353 Berlin, Germany; Institute of Cell and Neurobiology, Charité - Universitätsmedizin Berlin, Campus Mitte, Charitéplatz 1, 10115 Berlin, Germany.

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http://dx.doi.org/10.1016/j.ejpn.2013.08.008DOI Listing
January 2014

WITHDRAWN: Is microcephaly a so-far unrecognized feature of XYY syndrome?

Gene 2013 Sep 12. Epub 2013 Sep 12.

Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353 Berlin, Germany.

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http://dx.doi.org/10.1016/j.gene.2013.09.009DOI Listing
September 2013

Microcephaly.

Handb Clin Neurol 2013 ;111:129-41

Department of Genetics, Hôpital Robert Debré, Paris, France; Inserm U676 and Medical School, Denis Diderot-Paris VII University, Paris, France.

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http://dx.doi.org/10.1016/B978-0-444-52891-9.00013-0DOI Listing
April 2014

Combined deletion 18q22.2 and duplication/triplication 18q22.1 causes microcephaly, mental retardation and leukencephalopathy.

Gene 2013 Jul 5;523(1):92-8. Epub 2013 Apr 5.

Department of Pediatric Neurology, Charité-Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353 Berlin, Germany.

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http://dx.doi.org/10.1016/j.gene.2013.03.078DOI Listing
July 2013

Angelman syndrome and severe infections in a patient with de novo 15q11.2-q13.1 deletion and maternally inherited 2q21.3 microdeletion.

Gene 2013 Jan 1;512(2):453-5. Epub 2012 Nov 1.

Department of Pediatric Neurology, Charité, Universitätsmedizin Berlin, Germany.

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http://dx.doi.org/10.1016/j.gene.2012.10.061DOI Listing
January 2013

CDK5RAP2 expression during murine and human brain development correlates with pathology in primary autosomal recessive microcephaly.

Cereb Cortex 2013 Sep 17;23(9):2245-60. Epub 2012 Jul 17.

Institute of Cell Biology and Neurobiology, Charité - Universitätsmedizin Berlin, Berlin 10115, Germany.

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http://dx.doi.org/10.1093/cercor/bhs212DOI Listing
September 2013

Reference genes in the developing murine brain and in differentiating embryonic stem cells.

Neurol Res 2012 Sep 26;34(7):664-8. Epub 2012 Jun 26.

Institute of Neuroanatomy and Cell Biology, Charité - Universitätsmedizin Berlin, Germany.

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http://dx.doi.org/10.1179/1743132812Y.0000000060DOI Listing
September 2012

The yin and yang of microglia.

Dev Neurosci 2011 15;33(3-4):199-209. Epub 2011 Jul 15.

Department of Pediatric Neurology, Campus Virchow-Klinikum, Charité - Universitätsmedizin Berlin, Berlin, Germany.

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https://www.karger.com/Article/FullText/328989
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http://dx.doi.org/10.1159/000328989DOI Listing
March 2012

What's the hype about CDK5RAP2?

Cell Mol Life Sci 2011 May 17;68(10):1719-36. Epub 2011 Feb 17.

Department of Pediatric Neurology, Charité, Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany.

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http://dx.doi.org/10.1007/s00018-011-0635-4DOI Listing
May 2011

Neuronal death and oxidative stress in the developing brain.

Antioxid Redox Signal 2011 Apr 20;14(8):1535-50. Epub 2011 Feb 20.

Department of Neurology, University of Wisconsin, 600 Highland Avenue, Madison, WI 53792, USA.

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http://www.liebertpub.com/doi/10.1089/ars.2010.3581
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http://dx.doi.org/10.1089/ars.2010.3581DOI Listing
April 2011

Inflammation processes in perinatal brain damage.

J Neural Transm (Vienna) 2010 Aug 15;117(8):1009-17. Epub 2010 May 15.

Hôpital Robert Debré, Inserm, U676, 48 Blvd Serurier, 75019 Paris, France.

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http://dx.doi.org/10.1007/s00702-010-0411-xDOI Listing
August 2010

Common molecular causes for congenital heart defects and microcephaly.

Am J Obstet Gynecol 2010 Feb 4;202(2):e7; author reply e7-8. Epub 2009 Oct 4.

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https://linkinghub.elsevier.com/retrieve/pii/S00029378090096
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http://dx.doi.org/10.1016/j.ajog.2009.08.034DOI Listing
February 2010

Erythropoietin attenuates hyperoxia-induced cell death by modulation of inflammatory mediators and matrix metalloproteinases.

Dev Neurosci 2009 11;31(5):394-402. Epub 2009 Aug 11.

Department of Neonatology, Campus Virchow-Klinikum, Charité-Universitätsmedizin Berlin, Berlin, Germany.

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http://dx.doi.org/10.1159/000232557DOI Listing
November 2009

Molecular mechanisms involved in injury to the preterm brain.

J Child Neurol 2009 Sep 15;24(9):1112-8. Epub 2009 Jul 15.

Inserm, U676, Paris, France.

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http://dx.doi.org/10.1177/0883073809337920DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3743549PMC
September 2009

Erythropoietin protects the developing brain from hyperoxia-induced cell death and proteome changes.

Ann Neurol 2008 Nov;64(5):523-34

Department of Pediatric Neurology, Charité-Universitätsmedizin Berlin, Campus Virchow-Klinikum, Berlin, Germany.

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http://dx.doi.org/10.1002/ana.21471DOI Listing
November 2008

Sedative and anticonvulsant drugs suppress postnatal neurogenesis.

Ann Neurol 2008 Oct;64(4):434-45

Department of Pediatric Neurology, Children's Hospital, Medical Faculty Carl Gustav Carus, University of Technology Dresden, Dresden, Germany.

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http://dx.doi.org/10.1002/ana.21463DOI Listing
October 2008

Autosomal recessive primary microcephalies (MCPH).

Eur J Paediatr Neurol 2009 Sep 5;13(5):458. Epub 2008 Sep 5.

Inserm U676, Hôpital Robert Debré, 48 Bolevard Serurier, 75019 Paris, France.

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http://linkinghub.elsevier.com/retrieve/pii/S109037980800150
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http://dx.doi.org/10.1016/j.ejpn.2008.07.010DOI Listing
September 2009

Brief alteration of NMDA or GABAA receptor-mediated neurotransmission has long term effects on the developing cerebral cortex.

Mol Cell Proteomics 2008 Dec 27;7(12):2293-310. Epub 2008 Jun 27.

Department of Pediatric Neurology, Institute of Human Genetics, Charité-Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353 Berlin, Germany.

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http://www.mcponline.org/content/7/12/2293.full.pdf
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http://www.mcponline.org/cgi/doi/10.1074/mcp.M800030-MCP200
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http://dx.doi.org/10.1074/mcp.M800030-MCP200DOI Listing
December 2008

Spinal muscular atrophy with respiratory distress type 1 (SMARD1).

J Child Neurol 2008 Feb;23(2):199-204

Department of Pediatric Neurology, Charité, University Medical Center, Berlin, Germany.

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http://dx.doi.org/10.1177/0883073807310989DOI Listing
February 2008

Subacute proteome changes following traumatic injury of the developing brain: Implications for a dysregulation of neuronal migration and neurite arborization.

Proteomics Clin Appl 2007 Jul 6;1(7):640-9. Epub 2007 Jun 6.

Department of Pediatric Neurology, Charité, University Medicine Berlin, Campus Virchow-Klinikum, Berlin, Germany; Institute of Human Genetics, Charité, University Medicine Berlin, Campus Virchow-Klinikum, Berlin, Germany; Department of Pediatric Neurology, University Childrens' Hospital, Technical University Dresden, Dresden, Germany.

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http://doi.wiley.com/10.1002/prca.200600696
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http://dx.doi.org/10.1002/prca.200600696DOI Listing
July 2007

Glutamate antagonists are neurotoxins for the developing brain.

Neurotox Res 2007 Apr;11(3-4):203-18

Department of Pediatric Neurology, Charité, University Medical School, Campus Virchow-Klinikum, Augustenburger Platz 1,13353 Berlin, Germany.

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http://dx.doi.org/10.1007/BF03033568DOI Listing
April 2007

Selenoprotein N muscular dystrophy: differential diagnosis for early-onset limited mobility of the spine.

J Child Neurol 2006 Apr;21(4):316-20

Department of Pediatric Neurology, Children's Hospital Technical University Dresden, Germany.

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http://dx.doi.org/10.1177/08830738060210041401DOI Listing
April 2006

Comparative proteomics in neurodegenerative and non-neurodegenerative diseases suggest nodal point proteins in regulatory networking.

J Proteome Res 2006 Aug;5(8):1948-58

Institute of Human Genetics, Charité, University Medicine Berlin, Augustenbuger Platz 1, 13353 Berlin, Germany.

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http://dx.doi.org/10.1021/pr0601077DOI Listing
August 2006

Limb girdle muscular dystrophy type 2I caused by a novel missense mutation in the FKRP gene presenting as acute virus-associated myositis in infancy.

Eur J Pediatr 2006 Jan 6;165(1):62-3. Epub 2005 Sep 6.

Department of Paediatric Neurology, Children's Hospital, Technical University Dresden, Fetscherstrasse 74, 01307, Dresden, Germany.

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http://link.springer.com/10.1007/s00431-005-1752-6
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January 2006

Sulthiame but not levetiracetam exerts neurotoxic effect in the developing rat brain.

Exp Neurol 2005 Jun;193(2):497-503

Department of Pediatric Neurology, Charité, Virchow Clinics, Humboldt University, Augustenburger Platz 1, 13353 Berlin, Germany.

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http://dx.doi.org/10.1016/j.expneurol.2005.01.006DOI Listing
June 2005

High reproducibility of large-gel two-dimensional electrophoresis.

Electrophoresis 2004 Sep;25(17):3040-7

Institute for Theoretical Biology, Humboldt University, Berlin, Germany.

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http://dx.doi.org/10.1002/elps.200405979DOI Listing
September 2004