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American Journal of Medical Genetics|July 23, 1998
Clinical homogeneity of the Stüve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2V Cormier-Daire, A Superti-Furga, A Munnich, et al.
Pediatric Research|October 1, 1975
Persistent and transient distal renal tubular acidosis with bicarbonate wastingE P Leumann, B Steinmann
Schweizerische Medizinische Wochenschrift|May 26, 1979
[Catamnestic studies in hemiplegics]S Hasler-Kündig, B Steinmann
The Biochemical Journal|November 15, 1980
Reduced lysyl oxidase activity in skin fibroblasts from patients with Menkes' syndromeP M Royce, J Camakaris, D M Danks
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 10, 2025
Comprehensive genetic diagnosis and therapeutic perspectives in 155 children with developmental and epileptic encephalopathyR van Heurck, E B Hammar, D Ville, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|December 16, 2000
[Hereditary prolidase deficiency. Contribution to differential therapy refractory leg ulcer diagnosis]R Kasten, B Steinmann, V Voigtländer
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 15, 1983
Zonal differences of alpha-glucosidases in human kidney: studies in controls and in patients with glycogenosis type IIK Pfister, R Gitzelmann, B Steinmann
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