Publications by authors named "Johannes Lemke"

98Publications

Friend or Foe: S100 Proteins in Cancer.

Cancers (Basel) 2020 Jul 24;12(8). Epub 2020 Jul 24.

Department of General and Visceral Surgery, Ulm University Hospital, Albert-Einstein-Allee 23, 89081 Ulm, Germany.

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http://dx.doi.org/10.3390/cancers12082037DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465620PMC
July 2020

Predicting incidences of neurodevelopmental disorders.

Authors:
Johannes R Lemke

Brain 2020 04;143(4):1046-1048

Institute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany.

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http://dx.doi.org/10.1093/brain/awaa079DOI Listing
April 2020

Defining and expanding the phenotype of -associated developmental epileptic encephalopathy.

Neurol Genet 2019 Dec 10;5(6):e373. Epub 2019 Dec 10.

Department of Epilepsy Genetics and Precision Medicine (K.J.M., E.G., G.R., R.S.M.), The Danish Epilepsy Centre Filadelfia, Dianalund, Denmark; Institute for Regional Health Services (K.J.M., E.G., R.S.M.), University of Southern Denmark, Odense; Institute of Human Genetics (D.M., R. Jamra, A.F., J.R.L.), University of Leipzig Medical Center, Germany; Institute of Structural Biology (R. Janowski, D.N.), Helmholtz Zentrum München - German Research Center for Environmental Health, Neuherberg, Germany; Department of Paediatric Radiology (C.R.), University of Leipzig Medical Center, Germany; Department of Epilepsy, Sleep and Pediatric Neurophysiology (J.T.), Lyon University Hospital, France; Neuropediatric Unit (A.-L.P., D.M.V., G.L.), Lyon University Hospital, France; Department of Medical Genetics (N.C., G.L.), Lyon University Hospital, France; GenDev Team (N.C.), CNRS UMR 5292, INSERM U1028, CNRL and University of Lyon, France; Department of Genetics (E.B.), University Medical Center Utrecht, The Netherlands; Department of Child Neurology (K.G.), Brain Center Rudolf Magnus, University Medical Center Utrecht, The Netherlands; Department of Paediatrics (A.P.B.), Copenhagen University Hospital Rigshospitalet, Denmark; Baylor College of Medicine (S.M., K.N.), Children's Hospital of San Antonio; Undiagnosed Diseases Program (G.B., C.P.), Genetic Services of Western Australia, Department of Health, Government of Western Australia, Perth; Western Australian Register of Developmental Anomalies (G.B., D.G.), Australia; Telethon Kids Institute and the School of Paediatrics and Child Health (G.B.), University of Western Australia, Perth; Linear Clinical Research (L.D.), WA, Australia; Center of Human Genetics (S.S), Jena University Hospital, Germany; Department of Neuropediatrics (A.D.), Jena University Hospital, Germany; Division of Neurology (K.L.H.), Children's Hospital of Philadelphia, PA; Division of Neuropediatrics (A.M.), University of Leipzig Medical Center, Germany; Amplexa Genetics (H.H.), Odense, Denmark; Clinic for Children (H.H.), Værløse, Denmark; Center for Integrative Brain Research (G.M.), Seattle Children's Research Institute, WA; Department of Pediatrics (G.M.), University of Washington, Seattle; Medical Genetics Unit (F.B.), Department of Life, Health and Environmental Sciences, University of L'Aquila, Italy; Istituto Dermopatico dell'Immacolata (F.B.), IDI-IRCCS, Rome, Italy; Institute of Human Genetics (T.B., M.H.), University Medical Center Hamburg-Eppendorf, Germany; Childrens Hospital (J.D.), University Medical Center Hamburg-Eppendorf, Germany; University of Copenhagen (G.R.), Denmark; Institute for Human Genetics (P.M.), University Hospital Magdeburg, Germany; Children's Hospital A. Meyer (R.G., A.V.), University of Florence, Italy; and Institute of Pharmaceutical Biotechnology (D.N.), Ulm University, Germany.

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http://dx.doi.org/10.1212/NXG.0000000000000373DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927360PMC
December 2019

Genotype-phenotype correlation on 45 individuals with West syndrome.

Eur J Paediatr Neurol 2020 Mar 26;25:134-138. Epub 2019 Nov 26.

Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2019.11.010DOI Listing
March 2020

Association of Genomic Domains in and with Prostate Cancer Risk and Aggressiveness.

Authors:
Vivek L Patel Evan L Busch Tara M Friebel Angel Cronin Goska Leslie Lesley McGuffog Julian Adlard Simona Agata Bjarni A Agnarsson Munaza Ahmed Kristiina Aittomäki Elisa Alducci Irene L Andrulis Adalgeir Arason Norbert Arnold Grazia Artioli Brita Arver Bernd Auber Jacopo Azzollini Judith Balmaña Rosa B Barkardottir Daniel R Barnes Alicia Barroso Daniel Barrowdale Muriel Belotti Javier Benitez Birgitte Bertelsen Marinus J Blok Istvan Bodrogi Valérie Bonadona Bernardo Bonanni Davide Bondavalli Susanne E Boonen Julika Borde Ake Borg Angela R Bradbury Angela Brady Carole Brewer Joan Brunet Bruno Buecher Saundra S Buys Santiago Cabezas-Camarero Trinidad Caldés Almuth Caliebe Maria A Caligo Mariarosaria Calvello Ian G Campbell Ileana Carnevali Estela Carrasco Tsun L Chan Annie T W Chu Wendy K Chung Kathleen B M Claes Gemo Study Collaborators Embrace Collaborators Jackie Cook Laura Cortesi Fergus J Couch Mary B Daly Giuseppe Damante Esther Darder Rosemarie Davidson Miguel de la Hoya Lara Della Puppa Joe Dennis Orland Díez Yuan Chun Ding Nina Ditsch Susan M Domchek Alan Donaldson Bernd Dworniczak Douglas F Easton Diana M Eccles Rosalind A Eeles Hans Ehrencrona Bent Ejlertsen Christoph Engel D Gareth Evans Laurence Faivre Ulrike Faust Lídia Feliubadaló Lenka Foretova Florentia Fostira George Fountzilas Debra Frost Vanesa García-Barberán Pilar Garre Marion Gauthier-Villars Lajos Géczi Andrea Gehrig Anne-Marie Gerdes Paul Gesta Giuseppe Giannini Gord Glendon Andrew K Godwin David E Goldgar Mark H Greene Angelica M Gutierrez-Barrera Eric Hahnen Ute Hamann Jan Hauke Natalie Herold Frans B L Hogervorst Ellen Honisch John L Hopper Peter J Hulick KConFab Investigators Hebon Investigators Louise Izatt Agnes Jager Paul James Ramunas Janavicius Uffe Birk Jensen Thomas Dyrso Jensen Oskar Th Johannsson Esther M John Vijai Joseph Eunyoung Kang Karin Kast Johanna I Kiiski Sung-Won Kim Zisun Kim Kwang-Pil Ko Irene Konstantopoulou Gero Kramer Lotte Krogh Torben A Kruse Ava Kwong Mirjam Larsen Christine Lasset Charlotte Lautrup Conxi Lazaro Jihyoun Lee Jong Won Lee Min Hyuk Lee Johannes Lemke Fabienne Lesueur Annelie Liljegren Annika Lindblom Patricia Llovet Adria Lopez-Fernández Irene Lopez-Perolio Victor Lorca Jennifer T Loud Edmond S K Ma Phuong L Mai Siranoush Manoukian Veronique Mari Lynn Martin Laura Matricardi Noura Mebirouk Veronica Medici Hanne E J Meijers-Heijboer Alfons Meindl Arjen R Mensenkamp Clare Miller Denise Molina Gomes Marco Montagna Thea M Mooij Lidia Moserle Emmanuelle Mouret-Fourme Anna Marie Mulligan Katherine L Nathanson Marie Navratilova Heli Nevanlinna Dieter Niederacher Finn C Cilius Nielsen Liene Nikitina-Zake Kenneth Offit Edith Olah Olufunmilayo I Olopade Kai-Ren Ong Ana Osorio Claus-Eric Ott Domenico Palli Sue K Park Michael T Parsons Inge Sokilde Pedersen Bernard Peissel Ana Peixoto Pedro Pérez-Segura Paolo Peterlongo Annabeth Høgh Petersen Mary E Porteous Miguel Angel Pujana Paolo Radice Juliane Ramser Johanna Rantala Muhammad U Rashid Kerstin Rhiem Piera Rizzolo Mark E Robson Matti A Rookus Caroline M Rossing Kathryn J Ruddy Catarina Santos Claire Saule Rosa Scarpitta Rita K Schmutzler Hélène Schuster Leigha Senter Caroline M Seynaeve Payal D Shah Priyanka Sharma Vivian Y Shin Valentina Silvestri Jacques Simard Christian F Singer Anne-Bine Skytte Katie Snape Angela R Solano Penny Soucy Melissa C Southey Amanda B Spurdle Linda Steele Doris Steinemann Dominique Stoppa-Lyonnet Agostina Stradella Lone Sunde Christian Sutter Yen Y Tan Manuel R Teixeira Soo Hwang Teo Mads Thomassen Maria Grazia Tibiletti Marc Tischkowitz Silvia Tognazzo Amanda E Toland Stefania Tommasi Diana Torres Angela Toss Alison H Trainer Nadine Tung Christi J van Asperen Frederieke H van der Baan Lizet E van der Kolk Rob B van der Luijt Liselotte P van Hest Liliana Varesco Raymonda Varon-Mateeva Alessandra Viel Jeroen Vierstraete Roberta Villa Anna von Wachenfeldt Philipp Wagner Shan Wang-Gohrke Barbara Wappenschmidt Jeffrey N Weitzel Greet Wieme Siddhartha Yadav Drakoulis Yannoukakos Sook-Yee Yoon Cristina Zanzottera Kristin K Zorn Anthony V D'Amico Matthew L Freedman Mark M Pomerantz Georgia Chenevix-Trench Antonis C Antoniou Susan L Neuhausen Laura Ottini Henriette Roed Nielsen Timothy R Rebbeck

Cancer Res 2020 02 13;80(3):624-638. Epub 2019 Nov 13.

Harvard T.H. Chan School of Public Health, Boston, Massachusetts.

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http://dx.doi.org/10.1158/0008-5472.CAN-19-1840DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7553241PMC
February 2020

Novel synonymous and missense variants in FGFR1 causing Hartsfield syndrome.

Am J Med Genet A 2019 12 11;179(12):2447-2453. Epub 2019 Sep 11.

Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.

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http://dx.doi.org/10.1002/ajmg.a.61354DOI Listing
December 2019

Calcitonin concentrations in patients with chronic kidney disease on hemodialysis in reference to parathyroidectomy.

BMC Res Notes 2019 Jul 19;12(1):439. Epub 2019 Jul 19.

Department of General and Visceral Surgery, University Hospital Ulm, Albert-Einstein-Allee 23, 89081, Ulm, Germany.

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http://dx.doi.org/10.1186/s13104-019-4479-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642600PMC
July 2019

Can Met-PET/CT Predict Sporadic Multiglandular Hyperparathyroidism? Report of a Case and Review of the Literature.

Case Rep Endocrinol 2019 15;2019:1791740. Epub 2019 May 15.

Department of Nuclear Medicine, University Medical Center Ulm, Ulm, Germany.

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http://dx.doi.org/10.1155/2019/1791740DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541976PMC
May 2019

Parental mosaicism in epilepsies due to alleged de novo variants.

Epilepsia 2019 06 11;60(6):e63-e66. Epub 2019 May 11.

Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.

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http://dx.doi.org/10.1111/epi.15187DOI Listing
June 2019

TRAILblazing Strategies for Cancer Treatment.

Cancers (Basel) 2019 Mar 30;11(4). Epub 2019 Mar 30.

Department of General and Visceral Surgery, Ulm University Hospital, Albert-Einstein-Allee 23, 89081 Ulm, Germany.

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https://www.mdpi.com/2072-6694/11/4/456
Publisher Site
http://dx.doi.org/10.3390/cancers11040456DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521007PMC
March 2019

From next-generation sequencing to targeted treatment of non-acquired epilepsies.

Expert Rev Mol Diagn 2019 03 4;19(3):217-228. Epub 2019 Feb 4.

a Department of Epilepsy Genetics and Precision Medicine , The Danish Epilepsy Centre , Dianalund , Denmark.

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http://dx.doi.org/10.1080/14737159.2019.1573144DOI Listing
March 2019

Postoperative swallowing disorder after thyroid and parathyroid resection.

Pragmat Obs Res 2018 16;9:63-68. Epub 2018 Oct 16.

Department of General and Visceral Surgery, Ulm University Medical Center, 89081 Ulm, Germany,

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http://dx.doi.org/10.2147/POR.S172059DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198892PMC
October 2018

The Emerging Role of Cyclin-Dependent Kinases (CDKs) in Pancreatic Ductal Adenocarcinoma.

Int J Mol Sci 2018 Oct 18;19(10). Epub 2018 Oct 18.

Department of General and Visceral Surgery, Ulm University Hospital, Albert-Einstein-Allee 23, 89081 Ulm, Germany.

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http://dx.doi.org/10.3390/ijms19103219DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214075PMC
October 2018

Correction: The landscape of epilepsy-related GATOR1 variants.

Genet Med 2019 Aug;21(8):1896

Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013 Paris, France.

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http://dx.doi.org/10.1038/s41436-018-0325-9DOI Listing
August 2019

NfL is a biomarker for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia.

Neurology 2018 10 14;91(16):755-757. Epub 2018 Sep 14.

From the Department of Neurodegenerative Diseases (S.N.H., L.S.), Hertie-Institute for Clinical Brain Research & Center of Neurology, University of Tübingen, Germany; German Research Center for Neurodegenerative Diseases (DZNE) (S.N.H., L.S.), Tübingen, Germany; Institute of Human Genetics (I.K., F.R., J.R.L.), University of Leipzig, Germany; Neurologic Clinic and Policlinic, Departments of Medicine, Biomedicine and Clinical Research (C.B., J.K.), University Hospital Basel, University of Basel, Switzerland; and Department of Neurology (P.K.), University of Magdeburg, Germany.

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http://dx.doi.org/10.1212/WNL.0000000000006357DOI Listing
October 2018

Correction to: The landscape of epilepsy-related GATOR1 variants.

Genet Med 2019 Jul;21(7):1671

Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France.

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http://dx.doi.org/10.1038/s41436-018-0284-1DOI Listing
July 2019

Relationship of electrophysiological dysfunction and clinical severity in SCN2A-related epilepsies.

Hum Mutat 2018 12 13;39(12):1942-1956. Epub 2018 Sep 13.

Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, Tuebingen, Germany.

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http://dx.doi.org/10.1002/humu.23619DOI Listing
December 2018

The landscape of epilepsy-related GATOR1 variants.

Genet Med 2019 02 10;21(2):398-408. Epub 2018 Aug 10.

Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France.

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http://www.nature.com/articles/s41436-018-0060-2
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http://dx.doi.org/10.1038/s41436-018-0060-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292495PMC
February 2019

Should We Keep Walking along the Trail for Pancreatic Cancer Treatment? Revisiting TNF-Related Apoptosis-Inducing Ligand for Anticancer Therapy.

Cancers (Basel) 2018 Mar 18;10(3). Epub 2018 Mar 18.

Department of General and Visceral Surgery, Ulm University Hospital, Albert-Einstein-Allee 23, 89081 Ulm, Germany.

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http://dx.doi.org/10.3390/cancers10030077DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876652PMC
March 2018

Thyroid gland hemorrhage after blunt neck trauma: case report and review of the literature.

BMC Surg 2017 Nov 28;17(1):115. Epub 2017 Nov 28.

Department Surgery, Division of General and Visceral Surgery, Ulm University Medical Center, Albert-Einstein-Allee 23, 89081, Ulm, Germany.

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http://dx.doi.org/10.1186/s12893-017-0322-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706149PMC
November 2017

High-Throughput Sequencing as First-Tier Diagnostics in Congenital and Early-Onset Disorders.

Authors:
Johannes R Lemke

JAMA Pediatr 2017 09;171(9):833-835

Institute of Human Genetics, University of Leipzig Hospitals and Clinics, Leipzig, Germany.

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http://dx.doi.org/10.1001/jamapediatrics.2017.1970DOI Listing
September 2017

Commentary: GATOR Complex-Associated Epilepsies.

Authors:
Johannes R Lemke

Epilepsia 2017 07 14;58(7):1121-1122. Epub 2017 Jun 14.

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http://dx.doi.org/10.1111/epi.13789DOI Listing
July 2017

Copy number variations in "classical" obesity candidate genes are not frequently associated with severe early-onset obesity in children.

J Pediatr Endocrinol Metab 2017 May;30(5):507-515

Pediatric Research Center, University Hospital for Children and Adolescents, Medical Faculty, University of Leipzig, Leipzig.

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http://dx.doi.org/10.1515/jpem-2016-0435DOI Listing
May 2017

Vitamin B6-Responsive Epilepsy due to a Novel KCNQ2 Mutation.

Neuropediatrics 2017 Jun 18;48(3):199-204. Epub 2017 Apr 18.

Department of Neuropediatrics and Muscle Disorders, Center for Pediatrics, University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

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http://dx.doi.org/10.1055/s-0037-1601857DOI Listing
June 2017

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

Brain 2017 May;140(5):1316-1336

The Danish Epilepsy Centre, Dianalund, Denmark.

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http://dx.doi.org/10.1093/brain/awx054DOI Listing
May 2017

encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.

J Med Genet 2017 07 4;54(7):460-470. Epub 2017 Apr 4.

Institute of Human Genetics, University of Leipzig Hospitals and Clinics, Leipzig, Germany.

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http://dx.doi.org/10.1136/jmedgenet-2016-104509DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656050PMC
July 2017

Endogenously Expressed IL-4Rα Promotes the Malignant Phenotype of Human Pancreatic Cancer In Vitro and In Vivo.

Int J Mol Sci 2017 Mar 28;18(4). Epub 2017 Mar 28.

Department of General and Visceral Surgery, University of Ulm, Albert-Einstein-Allee 23, 89081 Ulm, Germany.

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http://www.mdpi.com/1422-0067/18/4/716
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http://dx.doi.org/10.3390/ijms18040716DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412302PMC
March 2017

CDK9 is a prognostic marker and therapeutic target in pancreatic cancer.

Tumour Biol 2017 Feb;39(2):1010428317694304

1 Department of General and Visceral Surgery, Center for Surgery, Ulm University Hospital, Ulm, Germany.

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http://dx.doi.org/10.1177/1010428317694304DOI Listing
February 2017

Mutations in GABRB3: From febrile seizures to epileptic encephalopathies.

Neurology 2017 01 4;88(5):483-492. Epub 2017 Jan 4.

From the Danish Epilepsy Centre (R.S.M., K.M.J., M.N.), Dianalund; Institute for Regional Health Services (R.S.M., K.M.J., M.N.), University of Southern Denmark, Odense; Department of Neurology and Epileptology (T.V.W., S.V., H.L., S.M.), Hertie Institute for Clinical Brain Research, and Department of Neurosurgery (T.V.W.), University of Tübingen; Department of Neuropediatrics (I.H., M.P., S.v.S., H.M.), University Medical Center Schleswig-Holstein, Kiel, Germany; Division of Neurology (I.H., S.H., H.D.), The Children's Hospital of Philadelphia, PA; Neuroscience Department (C.M., R.G.), Children's Hospital Anna Meyer-University of Florence, Italy; Department of Genetics (E.H.B., M.S., K.L.v.G.), University Medical Center Utrecht, the Netherlands; Department of Neurology and Neurorehabilitation (U.V., I.T., T.T.), Children's Clinic of Tartu University Hospital, Estonia; Department of Pediatric Neurology and Epilepsy Center (I.B.), LMU Munich, Germany; Department of Pediatrics (I.T., T.T.), University of Tartu; Tallinn Children's Hospital (I.T.), Tallinn, Estonia; Clinic for Neuropediatrics and Neurorehabilitation (G.K., C.B., H.H.), Epilepsy Center for Children and Adolescents, Schön Klinik Vogtareuth, Germany; Paracelsus Medical Private University (G.K.), Salzburg, Austria; Neuropeadiatric Department (L.L.F.), Hospices Civils de Lyon; Department of Genetics (G.L., N.C.), Lyon University Hospitals; Claude Bernard Lyon I University (G.L., N.C.); Lyon Neuroscience Research Centre (G.L., N.C.), CNRS UMR5292, INSERM U1028; Epilepsy, Sleep and Pediatric Neurophysiology Department (J.d.B.), Lyon University Hospitals, France; Clinic for Pediatric Neurology (S.B.), Pediatric Department, University Hospital, Herlev, Denmark; Kleinwachau (N.H.), Sächsisches Epilepsiezentrum Radeberg, Dresden; Department of Neuropediatrics/Epilepsy Center (J.J.), University Medical Center Freiburg; Department of General Paediatrics (S.S.), Division of Child Neurology and Inherited Metabolic Diseases, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg; Department of Women and Child Health (S.S.), Hospital for Children and Adolescents, University of Leipzig Hospitals and Clinics, Germany; Department of Pediatrics (C.T.M., H.C.M.), Division of Genetic Medicine, University of Washington, Seattle; Amplexa Genetics (L.H.G.L., H.A.D.), Odense, Denmark; Northern German Epilepsy Center for Children and Adolescents (S.v.S.), Schwentinental-Raisdorf, Germany; Wilhelm Johannsen Centre for Functional Genome Research (Y.M., N.T.), Department of Cellular and Molecular Medicine, University of Copenhagen; Danish Epilepsy Center (G.R.), Filadelfia/University of Copenhagen, Denmark; Department of Diagnostics (J.R.L.), Institute of Human Genetics, University of Leipzig; and Svt. Luka's Institute of Child Neurology and Epilepsy (K.M.), Moscow, Russia. Dr Maljevic is currently at the Florey Institute of Neuroscience and Mental Health, Melbourne, Australia.

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http://dx.doi.org/10.1212/WNL.0000000000003565DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278942PMC
January 2017

Reply.

Ann Neurol 2017 02;81(2):328-329

Institute of Human Genetics, University of Leipzig Hospitals and Clinics, Leipzig, Germany.

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http://dx.doi.org/10.1002/ana.24856DOI Listing
February 2017

Multigene panel next generation sequencing in a patient with cherry red macular spot: Identification of two novel mutations in gene causing sialidosis type I associated with mild to unspecific biochemical and enzymatic findings.

Mol Genet Metab Rep 2017 Mar 1;10:1-4. Epub 2016 Dec 1.

Hospital for Children and Adolescents, Centre for Pediatric Research Leipzig (CPL), Department of Women and Child Health, University Hospitals, University of Leipzig, Liebigstraße 20 a, 04103 Leipzig, Germany.

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https://linkinghub.elsevier.com/retrieve/pii/S22144269163007
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http://dx.doi.org/10.1016/j.ymgmr.2016.11.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5137178PMC
March 2017

Challenging the limits in pancreatic surgery: A case report.

Int J Surg Case Rep 2016 15;29:151-154. Epub 2016 Nov 15.

Department of General and Visceral Surgery, University of Ulm, Albert-Einstein-Allee 23, 89081 Ulm, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.ijscr.2016.10.062DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114584PMC
November 2016

Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome.

Mol Syndromol 2016 Sep 24;7(4):239-246. Epub 2016 Aug 24.

Institute of Human Genetics, University Hospital and Clinics, Leipzig, Germany.

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http://dx.doi.org/10.1159/000448445DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073659PMC
September 2016

Novel Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures.

Mol Syndromol 2016 Sep 7;7(4):189-196. Epub 2016 Jul 7.

Department of Women and Child Health, Hospital for Children and Adolescents, Heidelberg, Germany; Division of Child Neurology and Inherited Metabolic Diseases, Department of General Pediatrics, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.

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https://www.karger.com/Article/FullText/447461
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http://dx.doi.org/10.1159/000447461DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073621PMC
September 2016

Towards a Molecular Syndromology of the Epilepsies.

Mol Syndromol 2016 Sep 17;7(4):169-171. Epub 2016 Aug 17.

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http://dx.doi.org/10.1159/000448358DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073502PMC
September 2016

Survival and Prognostic Factors of Colorectal Liver Metastases After Surgical and Nonsurgical Treatment.

Clin Colorectal Cancer 2016 12 7;15(4):e183-e192. Epub 2016 May 7.

Clinic of General and Visceral Surgery, University of Ulm, Ulm, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.clcc.2016.04.007DOI Listing
December 2016

Reply.

Ann Neurol 2016 07 10;80(1):168-9. Epub 2016 May 10.

Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.

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http://dx.doi.org/10.1002/ana.24669DOI Listing
July 2016

Management of a giant perineal condylomata acuminata.

GMS Interdiscip Plast Reconstr Surg DGPW 2016 21;5:Doc07. Epub 2016 Jan 21.

Clinic of General and Visceral Surgery, University of Ulm, Ulm, Germany.

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http://dx.doi.org/10.3205/iprs000086DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724757PMC
January 2016

Decreased CK1δ expression predicts prolonged survival in colorectal cancer patients.

Tumour Biol 2016 Jul 7;37(7):8731-9. Epub 2016 Jan 7.

Department of General and Visceral Surgery, Surgery Centre, Ulm University Hospital, Albert-Einstein-Allee 23, 89081, Ulm, Germany.

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http://dx.doi.org/10.1007/s13277-015-4745-8DOI Listing
July 2016

Ectopic spleen and liver hemangioma mimicking metastatic pancreatic neuroendocrine tumor.

Int J Surg Case Rep 2015 6;17:139-42. Epub 2015 Nov 6.

Clinic of General and Visceral Surgery, University of Ulm, Albert-Einstein-Allee 23, 89081 Ulm, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.ijscr.2015.10.041DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4701808PMC
January 2016

From Genetics to Genomics: A Short Introduction for Pediatric Neurologists.

Neuropediatrics 2016 Jan 16;47(1):5-11. Epub 2015 Nov 16.

Institut für Humangenetik, Universitätsklinikum Leipzig, Leipzig, Germany.

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http://dx.doi.org/10.1055/s-0035-1566448DOI Listing
January 2016

Tentative clinical diagnosis of Lujan-Fryns syndrome--A conglomeration of different genetic entities?

Am J Med Genet A 2016 Jan 11;170A(1):94-102. Epub 2015 Sep 11.

Institut fuer Klinische Genetik, Medizinische Fakultaet Carl Gustav Carus, Technische Universitaet Dresden, Dresden, Germany.

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http://dx.doi.org/10.1002/ajmg.a.37378DOI Listing
January 2016

Investigation of GRIN2A in common epilepsy phenotypes.

Epilepsy Res 2015 Sep 2;115:95-9. Epub 2015 Jun 2.

Division of Human Genetics, University Children's Hospital Inselspital, Bern, Switzerland; Institute of Human Genetics, University Medical Center Leipzig, Leipzig, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.eplepsyres.2015.05.010DOI Listing
September 2015

Quality of Life After Sphincter-Preserving Rectal Cancer Resection.

Clin Colorectal Cancer 2015 Dec 6;14(4):e33-40. Epub 2015 Jun 6.

Clinic of General and Visceral Surgery, University of Ulm, Ulm, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.clcc.2015.05.012DOI Listing
December 2015

Epileptic Encephalopathies in Childhood: The Role of Genetic Testing.

Semin Neurol 2015 Jun 10;35(3):310-22. Epub 2015 Jun 10.

Department of Women and Child Health, Hospital for Children and Adolescents, University of Leipzig, Leipzig, Germany.

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http://dx.doi.org/10.1055/s-0035-1552623DOI Listing
June 2015