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British Medical Journal (Clinical Research Ed.)|November 9, 1985
Controlled trial of methylprednisolone pulses and low dose oral prednisone for the minimal change nephrotic syndromeE Imbasciati, R Gusmano, A Edefonti, et al.
The Journal of Investigative Dermatology|May 1, 1996
Fibrillin and elastin expression in skin regenerating from cultured keratinocyte autografts: morphogenesis of microfibrils begins at the dermo-epidermal junction and precedes elastic fiber formationM Raghunath, T Bächi, M Meuli, et al.
Deutsche Medizinische Wochenschrift (1946)|June 24, 1983
[Infusion-associated kidney and liver failure in undiagnosed hereditary fructose intolerance]D E Müller-Wiefel, B Steinmann, M Holm-Hadulla, et al.
American Journal of Human Genetics|January 1, 1997
Duplication of seven exons in the lysyl hydroxylase gene is associated with longer forms of a repetitive sequence within the gene and is a common cause for the type VI variant of Ehlers-Danlos syndromeJ Heikkinen, T Toppinen, H Yeowell, et al.
Human Genetics|November 1, 1994
Three unrelated individuals with perinatally lethal osteogenesis imperfecta resulting from identical Gly502Ser substitutions in the alpha 2-chain of type I collagenN J Rose, K Mackay, A De Paepe, et al.
Helvetica Paediatrica Acta|February 1, 1978
Nonketotic hyperglycinemia treated with strychnine, a glycine receptor antagonistR Gitzelmann, B Steinmann, A Otten, et al.
The Journal of Biological Chemistry|September 25, 1980
Evidence for a structural mutation of procollagen type I in a patient with the Ehlers-Danlos syndrome type VIIB Steinmann, L Tuderman, L Peltonen, et al.
European Journal of Pediatrics|August 1, 1988
Lethal osteogenesis imperfecta: abnormal collagen metabolism and biochemical characteristics of hypophosphatasiaP M Royce, A Blumberg, R P Zurbrügg, et al.
Helvetica Paediatrica Acta|January 1, 1979
Congenital defect in intracellular cobalamin metabolism resulting in homocystinuria and methylmalonic aciduria. II. Biochemical investigationsE R Baumgartner, H Wick, J C Linnell, et al.
Clinical Nephrology|August 1, 1996
Children on continuous ambulatorial peritoneal dialysis: muscle and plasma proteins, amino acids and nutritional statusA Canepa, J C Divino Filho, A M Forsberg, et al.
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