Arpad von Moers

Arpad von Moers

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Arpad von Moers

Arpad von Moers

Publications by authors named "Arpad von Moers"

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Inflammation-induced fibrosis in skeletal muscle of female carriers of Duchenne muscular dystrophy.

Neuromuscul Disord 2019 Jul 10;29(7):487-496. Epub 2019 May 10.

Department of Neuropathology, Charité - Universitätsmedizin, Charité Campus Mitte, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health (BIH), Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.nmd.2019.05.003DOI Listing
July 2019

Abuse as a Cause of Childhood Fractures.

Dtsch Arztebl Int 2018 11;115(46):769-775

DRK Kliniken Berlin | Westend, Department of Pediatrics, Child Protection Outpatient Clinic; DRK Kliniken Berlin | Westend, Department of Diagnostic and Interventional Radiology; DRK Kliniken Berlin | Westend, Department of Trauma Surgery and Orthopedics; Department of Child and Adolescent Psychiatry/Psychotherapy.

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http://dx.doi.org/10.3238/arztebl.2018.0769DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329369PMC
November 2018

The Curse of Apneic Spells.

Semin Pediatr Neurol 2018 07 13;26:56-58. Epub 2017 Apr 13.

(⁎)Department of Neuropathology, Charité Universitätsmedizin Berlin, Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.spen.2017.03.006DOI Listing
July 2018

HaNDL Syndrome with Fever in a 12-Year-Old Boy - A Case Report.

Headache 2018 04 5;58(4):597-598. Epub 2018 Feb 5.

Department of Pediatrics, DRK Kliniken Berlin | Westend, Berlin, Germany.

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http://dx.doi.org/10.1111/head.13278DOI Listing
April 2018

Differential roles of hypoxia and innate immunity in juvenile and adult dermatomyositis.

Acta Neuropathol Commun 2016 04 27;4(1):45. Epub 2016 Apr 27.

Department of Neuropathology, Charité - Universitätsmedizin Berlin, Charité Campus Mitte, Charitéplatz 1, D-10117, Berlin, Germany.

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http://dx.doi.org/10.1186/s40478-016-0308-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847347PMC
April 2016

Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsy.

Neurol Genet 2015 Dec 22;1(4):e32. Epub 2015 Oct 22.

Departments of Neuropediatrics (G.S., D.S., F.S., S.M.-G., E.G., M.S.) and Neuropediatrics/SPZ (K.v.A.), NeuroCure Clinical Research Center, Charité-Universitätsmedizin, Berlin, Germany; the Department of Neuropathology (W.S.), Charité-Universitätsmedizin Berlin, Germany; and the DRK Children's Hospital Berlin (A.v.M.), Germany.

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http://ng.neurology.org/lookup/doi/10.1212/NXG.0000000000000
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http://dx.doi.org/10.1212/NXG.0000000000000032DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811389PMC
December 2015

Clinical application of whole exome sequencing reveals a novel compound heterozygous TK2-mutation in two brothers with rapidly progressive combined muscle-brain atrophy, axonal neuropathy, and status epilepticus.

Mitochondrion 2015 Jan 4;20:1-6. Epub 2014 Nov 4.

NeuroCure Clinical Research Center (NCRC), Charité-Universitätsmedizin Berlin, Germany; Department of Neuropediatrics, Charité-Universitätsmedizin Berlin, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.mito.2014.10.007DOI Listing
January 2015

Models for transition clinics.

Epilepsia 2014 Aug;55 Suppl 3:46-51

University of Antioquia, Medellín, Colombia.

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http://dx.doi.org/10.1111/epi.12716DOI Listing
August 2014

[Magnetic resonance imaging (MRI) in children and adolescents – study design of a feasibility study concerning examination related emotions].

Z Kinder Jugendpsychiatr Psychother 2013 Nov;41(6):447-51

Klinik für Psychiatrie, Psychosomatik und Psychotherapie des Kindes- und Jugendalters, CVK, Charité-Universitätsmedizin Berlin.

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https://econtent.hogrefe.com/doi/10.1024/1422-4917/a000260
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http://dx.doi.org/10.1024/1422-4917/a000260DOI Listing
November 2013

Atypical manifestation of childhood primary cerebral lymphoma restricted to the leptomeninges.

Eur J Pediatr 2005 Oct 26;164(10):653-4. Epub 2005 Jul 26.

Department of Neuropaediatrics, Charité University Medical School, Augustenburger Platz 1, 13353 Berlin, Germany.

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http://dx.doi.org/10.1007/s00431-005-1734-8DOI Listing
October 2005

Extended clinical phenotype, endocrine investigations and functional studies of a loss-of-function mutation A150V in the thyroid hormone specific transporter MCT8.

Eur J Endocrinol 2005 Sep;153(3):359-66

Department of Pediatric Endocrinology, Charité Children's Hospital, Humboldt University Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

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http://dx.doi.org/10.1530/eje.1.01980DOI Listing
September 2005

Delayed or late-onset type II glycogenosis with globular inclusions.

Acta Neuropathol 2005 Aug 29;110(2):151-7. Epub 2005 Jun 29.

Department of Neuropathology, Johannes Gutenberg University, Langenbeckstrasse 1, 55131, Mainz, Germany.

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http://link.springer.com/content/pdf/10.1007/s00401-005-1026
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http://link.springer.com/10.1007/s00401-005-1026-4
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http://dx.doi.org/10.1007/s00401-005-1026-4DOI Listing
August 2005

Increased mRNA expression of tissue inhibitors of metalloproteinase-1 and -2 in Duchenne muscular dystrophy.

Acta Neuropathol 2005 Mar 23;109(3):285-93. Epub 2004 Dec 23.

Department of Neuropediatrics, Charité, University Medical Center Berlin, Augustenburger Platz 1, 13353, Berlin, Germany.

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http://link.springer.com/10.1007/s00401-004-0941-0
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http://dx.doi.org/10.1007/s00401-004-0941-0DOI Listing
March 2005

Spontaneous scalp arteriovenous fistula in a child with hartnup disease.

J Endovasc Ther 2004 Jun;11(3):348-50

Department of Maxillo-Facial Surgery, Charité, Humboldt University, Berlin, Germany.

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http://jet.sagepub.com/lookup/doi/10.1583/03-1123.1
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http://dx.doi.org/10.1583/03-1123.1DOI Listing
June 2004

Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy.

Hum Genet 2004 Jan 5;114(2):149-56. Epub 2003 Nov 5.

Department of Neuropediatrics, Charité, Humboldt-University Berlin, Augustenburger Platz 1, 13353 Berlin, Germany.

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http://dx.doi.org/10.1007/s00439-003-1041-2DOI Listing
January 2004

Congenital disorder of glycosylation type 1a in a macrosomic 16-month-old boy with an atypical phenotype and homozygosity of the N216I mutation.

Eur J Pediatr 2003 Oct 2;162(10):710-3. Epub 2003 Aug 2.

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

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http://dx.doi.org/10.1007/s00431-003-1278-8DOI Listing
October 2003

MR imaging features in Marinesco-Sjögren syndrome: severe cerebellar atrophy is not an obligatory finding.

AJNR Am J Neuroradiol 2003 May;24(5):825-8

Clinic for Pediatric Neurology, Institute for Human Genetics, Charité Campus Virchow, Berlin, Germany.

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http://www.ajnr.org/content/24/5/825.full.pdf
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May 2003

EEG features of glut-1 deficiency syndrome.

Epilepsia 2002 Aug;43(8):941-5

Department of Pediatrics and Neuropediatrics, Charité Campus Virchow, Humboldt University, Berlin, Germany.

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http://dx.doi.org/10.1046/j.1528-1157.2002.50401.xDOI Listing
August 2002