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Hans-Jürgen Christen

Showing results (1-10 of 14) with videos related to

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Deutsches Arzteblatt International|June 30, 2009
Lyme disease--current state of knowledgeRoland Nau, Hans-Jürgen Christen, Helmut Eiffert
HNO|April 12, 2022
[Results of vagus nerve stimulator implantation in children and adolescents with treatment-refractory epilepsy]Kim Vanessa Steinke, Hartmut Möbius, Hans-Jürgen Christen, et al.
Human Mutation|August 31, 2006
Identification of the microdeletion breakpoint in a GLRA1null allele of Turkish hyperekplexia patientsKristina Becker, Carsten Hohoff, Bernhard Schmitt, et al.
Neuromuscular Disorders : NMD|October 16, 2004
A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndromeJuliane S Müller, Angela Abicht, Hans-Jürgen Christen, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathyKati Donner, Miina Ollikainen, Maaret Ridanpää, et al.
Neuropediatrics|April 10, 2025
MOG-Encephalitis is the Most Prevalent Autoimmune Encephalitis in Children: MERIN Study Data on EncephalitisRuth Helena Fellmeth, Lampros Kousoulos, George Christoph Korenke, et al.
European Journal of Human Genetics : EJHG|January 13, 2011
SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiencyLars Schlotawa, Eva Charlotte Ennemann, Karthikeyan Radhakrishnan, et al.
Deutsches Arzteblatt International|September 1, 2017
Acute Flaccid Myelitis in German Children in 2016-the Return of Polio?Johannes Hübner, Bernd Kruse, Hans-Jürgen Christen, et al.
Developmental Medicine and Child Neurology|May 13, 2014
Horizontal head titubation in infants with Joubert syndrome: a new findingAndrea Poretti, Hans-Jürgen Christen, Lindsay E Elton, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Ullrich congenital muscular dystrophy: connective tissue abnormalities in the skin support overlap with Ehlers-Danlos syndromesJanbernd Kirschner, Ingrid Hausser, Yaqun Zou, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Deutsches Arzteblatt International|June 30, 2009
Lyme disease--current state of knowledgeRoland Nau, Hans-Jürgen Christen, Helmut Eiffert
HNO|April 12, 2022
[Results of vagus nerve stimulator implantation in children and adolescents with treatment-refractory epilepsy]Kim Vanessa Steinke, Hartmut Möbius, Hans-Jürgen Christen, et al.
Human Mutation|August 31, 2006
Identification of the microdeletion breakpoint in a GLRA1null allele of Turkish hyperekplexia patientsKristina Becker, Carsten Hohoff, Bernhard Schmitt, et al.
Neuromuscular Disorders : NMD|October 16, 2004
A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndromeJuliane S Müller, Angela Abicht, Hans-Jürgen Christen, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathyKati Donner, Miina Ollikainen, Maaret Ridanpää, et al.
Neuropediatrics|April 10, 2025
MOG-Encephalitis is the Most Prevalent Autoimmune Encephalitis in Children: MERIN Study Data on EncephalitisRuth Helena Fellmeth, Lampros Kousoulos, George Christoph Korenke, et al.
European Journal of Human Genetics : EJHG|January 13, 2011
SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiencyLars Schlotawa, Eva Charlotte Ennemann, Karthikeyan Radhakrishnan, et al.
Deutsches Arzteblatt International|September 1, 2017
Acute Flaccid Myelitis in German Children in 2016-the Return of Polio?Johannes Hübner, Bernd Kruse, Hans-Jürgen Christen, et al.
Developmental Medicine and Child Neurology|May 13, 2014
Horizontal head titubation in infants with Joubert syndrome: a new findingAndrea Poretti, Hans-Jürgen Christen, Lindsay E Elton, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Ullrich congenital muscular dystrophy: connective tissue abnormalities in the skin support overlap with Ehlers-Danlos syndromesJanbernd Kirschner, Ingrid Hausser, Yaqun Zou, et al.
Pageof 2