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Journal of Child Neurology
|
May 1, 1999
Limb-girdle muscular dystrophies: an overview
C G Bönnemann
American Journal of Medical Genetics
|
June 14, 1996
Bilateral porencephaly, cerebellar hypoplasia, and internal malformations: two siblings representing a probably new autosomal recessive entity
C G Bönnemann, P Meinecke
Journal of Medical Genetics
|
April 1, 1990
Fetal brain disruption sequence: a milder variant
C G Bönnemann, P Meinecke
Neuropediatrics
|
June 1, 1992
Encephalopathy of infancy with intracerebral calcification and chronic spinal fluid lymphocytosis--another case of the Aicardi-Goutières syndrome
C G Bönnemann, P Meinecke
Clinical Dysmorphology
|
January 1, 1992
Microgastria-hypoplastic upper limb association: a severe expression including microphthalmia, single nostril and arhinencephaly
P Meinecke, C G Bönnemann, R Laas
Journal of Medical Genetics
|
October 1, 1991
Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration: two sibs confirming a probably distinct entity
C G Bönnemann, P Meinecke, H Reich
Neuropediatrics
|
December 19, 2003
Muscle ultrasound in Bethlem myopathy
C G Bönnemann, K Brockmann, F Hanefeld
Neuromuscular Disorders : NMD
|
March 8, 2016
212th ENMC International Workshop: Animal models of congenital muscular dystrophies, Naarden, The Netherlands, 29-31 May 2015
M Saunier, C G Bönnemann, M Durbeej, et al.
Neuromuscular Disorders : NMD
|
June 7, 2011
173rd ENMC International Workshop: congenital muscular dystrophy outcome measures 5-7 March 2010, Naarden, The Netherlands
C G Bönnemann, A Rutkowski, E Mercuri, et al.
Current Opinion in Pediatrics
|
December 1, 1996
Beyond dystrophin: current progress in the muscular dystrophies
C G Bönnemann, E M McNally, L M Kunkel
Page
of 5
Search research articles
Search
Showing results (1-10 of 42) with videos related to
Sort By:
Page
of 5
Journal of Child Neurology
|
May 1, 1999
Limb-girdle muscular dystrophies: an overview
C G Bönnemann
American Journal of Medical Genetics
|
June 14, 1996
Bilateral porencephaly, cerebellar hypoplasia, and internal malformations: two siblings representing a probably new autosomal recessive entity
C G Bönnemann, P Meinecke
Journal of Medical Genetics
|
April 1, 1990
Fetal brain disruption sequence: a milder variant
C G Bönnemann, P Meinecke
Neuropediatrics
|
June 1, 1992
Encephalopathy of infancy with intracerebral calcification and chronic spinal fluid lymphocytosis--another case of the Aicardi-Goutières syndrome
C G Bönnemann, P Meinecke
Clinical Dysmorphology
|
January 1, 1992
Microgastria-hypoplastic upper limb association: a severe expression including microphthalmia, single nostril and arhinencephaly
P Meinecke, C G Bönnemann, R Laas
Journal of Medical Genetics
|
October 1, 1991
Encephalopathy with intracerebral calcification, white matter lesions, growth hormone deficiency, microcephaly, and retinal degeneration: two sibs confirming a probably distinct entity
C G Bönnemann, P Meinecke, H Reich
Neuropediatrics
|
December 19, 2003
Muscle ultrasound in Bethlem myopathy
C G Bönnemann, K Brockmann, F Hanefeld
Neuromuscular Disorders : NMD
|
March 8, 2016
212th ENMC International Workshop: Animal models of congenital muscular dystrophies, Naarden, The Netherlands, 29-31 May 2015
M Saunier, C G Bönnemann, M Durbeej, et al.
Neuromuscular Disorders : NMD
|
June 7, 2011
173rd ENMC International Workshop: congenital muscular dystrophy outcome measures 5-7 March 2010, Naarden, The Netherlands
C G Bönnemann, A Rutkowski, E Mercuri, et al.
Current Opinion in Pediatrics
|
December 1, 1996
Beyond dystrophin: current progress in the muscular dystrophies
C G Bönnemann, E M McNally, L M Kunkel
Page
of 5