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Fortschritte Der Neurologie-Psychiatrie
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January 21, 2015
[Myotonic dystrophies: clinical presentation, pathogenesis, diagnostics and therapy]
Josef Finsterer, S Rudnik-Schöneborn
Kidney & Blood Pressure Research
|
January 1, 1996
Current status of DNA diagnosis for hereditary nephropathies
K Zerres, S Rudnik-Schöneborn
Archives of Neurology
|
May 1, 1995
Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classifications
K Zerres, S Rudnik-Schöneborn
Journal of Medical Genetics
|
June 1, 1994
A further patient with Pai syndrome with autosomal dominant inheritance?
S Rudnik-Schöneborn, K Zerres
Clinical Genetics
|
May 1, 1995
Course of autosomal recessive polycystic kidney disease (ARPKD) in siblings: a clinical comparison of 20 sibships
F Deget, S Rudnik-Schöneborn, K Zerres
Clinical Nephrology
|
October 13, 2001
DNA diagnosis in hereditary nephropathies
K Zerres, T Eggermann, S Rudnik-Schöneborn
Neuromuscular Disorders : NMD
|
May 1, 1997
Spinal muscular atrophy--clinical and genetic correlations
K Zerres, B Wirth, S Rudnik-Schöneborn
Human Genetics
|
June 1, 1994
Autosomal recessive polycystic kidney disease does not map to the second gene locus for autosomal dominant polycystic kidney disease on chromosome 4
K Zerres, G Mücher, S Rudnik-Schöneborn
American Journal of Human Genetics
|
July 1, 1994
Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophy
S Rudnik-Schöneborn, B Wirth, K Zerres
Journal of Medical Genetics
|
July 1, 1993
Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie
K Zerres, S Rudnik-Schöneborn, F Deget
Page
of 9
Search research articles
Search
Showing results (1-10 of 82) with videos related to
Sort By:
Page
of 9
Fortschritte Der Neurologie-Psychiatrie
|
January 21, 2015
[Myotonic dystrophies: clinical presentation, pathogenesis, diagnostics and therapy]
Josef Finsterer, S Rudnik-Schöneborn
Kidney & Blood Pressure Research
|
January 1, 1996
Current status of DNA diagnosis for hereditary nephropathies
K Zerres, S Rudnik-Schöneborn
Archives of Neurology
|
May 1, 1995
Natural history in proximal spinal muscular atrophy. Clinical analysis of 445 patients and suggestions for a modification of existing classifications
K Zerres, S Rudnik-Schöneborn
Journal of Medical Genetics
|
June 1, 1994
A further patient with Pai syndrome with autosomal dominant inheritance?
S Rudnik-Schöneborn, K Zerres
Clinical Genetics
|
May 1, 1995
Course of autosomal recessive polycystic kidney disease (ARPKD) in siblings: a clinical comparison of 20 sibships
F Deget, S Rudnik-Schöneborn, K Zerres
Clinical Nephrology
|
October 13, 2001
DNA diagnosis in hereditary nephropathies
K Zerres, T Eggermann, S Rudnik-Schöneborn
Neuromuscular Disorders : NMD
|
May 1, 1997
Spinal muscular atrophy--clinical and genetic correlations
K Zerres, B Wirth, S Rudnik-Schöneborn
Human Genetics
|
June 1, 1994
Autosomal recessive polycystic kidney disease does not map to the second gene locus for autosomal dominant polycystic kidney disease on chromosome 4
K Zerres, G Mücher, S Rudnik-Schöneborn
American Journal of Human Genetics
|
July 1, 1994
Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophy
S Rudnik-Schöneborn, B Wirth, K Zerres
Journal of Medical Genetics
|
July 1, 1993
Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie
K Zerres, S Rudnik-Schöneborn, F Deget
Page
of 9