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Der Nervenarzt
|
August 19, 2018
[Transition from neuropediatrics to neurology in neuromuscular diseases]
U Schara, G R Fink, A von Moers
Acta Paediatrica (Oslo, Norway : 1992)
|
April 1, 1997
Serum levels of carboxyterminal propeptide of type I procollagen, aminoterminal propeptide of type III procollagen and laminin P1 in Duchenne muscular dystrophy
A von Moers, T Danne, P Möller, et al.
Neuropediatrics
|
April 4, 2002
Large cerebral vessel occlusive disease in Lyme neuroborreliosis
R Klingebiel, G Benndorf, M Schmitt, et al.
Annals of Neurology
|
October 20, 1998
Epilepsia partialis continua associated with a homoplasmic mitochondrial tRNA(Ser(UCN)) mutation
M Schuelke, M Bakker, G Stoltenburg, et al.
Developmental Medicine and Child Neurology
|
September 1, 1991
Variable course of Canavan disease in two boys with early infantile aspartoacylase deficiency
A von Moers, J Sperner, T Michael, et al.
Neuropediatrics
|
December 1, 1992
Neuropathy with lysosomal changes in Marinesco-Sjögren syndrome: fine structural findings in skeletal muscle and conjunctiva
C Zimmer, G Gosztonyi, J Cervos-Navarro, et al.
Pediatric Cardiology
|
May 2, 1998
X-chromosomal (p21) muscular dystrophy and left ventricular diastolic and systolic function
K Brockmeier, L Schmitz, A von Moers, et al.
Medizinische Klinik (Munich, Germany : 1983)
|
April 1, 1995
[BiPAP therapy of respiratory disorders in patients with congenital neuromuscular diseases]
H Müller-Pawlowski, A von Moers, M Raffenberg, et al.
Neurology
|
November 30, 2000
Ataxia with vitamin E deficiency: biochemical effects of malcompliance with vitamin E therapy
M Schuelke, B Finckh, E A Sistermans, et al.
Pediatric Radiology
|
January 1, 1993
Cranial ultrasound findings in aspartoacylase deficiency (Canavan disease)
C Bührer, C Bassir, A von Moers, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Der Nervenarzt
|
August 19, 2018
[Transition from neuropediatrics to neurology in neuromuscular diseases]
U Schara, G R Fink, A von Moers
Acta Paediatrica (Oslo, Norway : 1992)
|
April 1, 1997
Serum levels of carboxyterminal propeptide of type I procollagen, aminoterminal propeptide of type III procollagen and laminin P1 in Duchenne muscular dystrophy
A von Moers, T Danne, P Möller, et al.
Neuropediatrics
|
April 4, 2002
Large cerebral vessel occlusive disease in Lyme neuroborreliosis
R Klingebiel, G Benndorf, M Schmitt, et al.
Annals of Neurology
|
October 20, 1998
Epilepsia partialis continua associated with a homoplasmic mitochondrial tRNA(Ser(UCN)) mutation
M Schuelke, M Bakker, G Stoltenburg, et al.
Developmental Medicine and Child Neurology
|
September 1, 1991
Variable course of Canavan disease in two boys with early infantile aspartoacylase deficiency
A von Moers, J Sperner, T Michael, et al.
Neuropediatrics
|
December 1, 1992
Neuropathy with lysosomal changes in Marinesco-Sjögren syndrome: fine structural findings in skeletal muscle and conjunctiva
C Zimmer, G Gosztonyi, J Cervos-Navarro, et al.
Pediatric Cardiology
|
May 2, 1998
X-chromosomal (p21) muscular dystrophy and left ventricular diastolic and systolic function
K Brockmeier, L Schmitz, A von Moers, et al.
Medizinische Klinik (Munich, Germany : 1983)
|
April 1, 1995
[BiPAP therapy of respiratory disorders in patients with congenital neuromuscular diseases]
H Müller-Pawlowski, A von Moers, M Raffenberg, et al.
Neurology
|
November 30, 2000
Ataxia with vitamin E deficiency: biochemical effects of malcompliance with vitamin E therapy
M Schuelke, B Finckh, E A Sistermans, et al.
Pediatric Radiology
|
January 1, 1993
Cranial ultrasound findings in aspartoacylase deficiency (Canavan disease)
C Bührer, C Bassir, A von Moers, et al.
Page
of 2