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European Journal of Pediatrics|May 1, 1988
The neonatal pseudo-hydrocephalic progeroid syndrome (Wiedemann-Rautenstrauch). Report of a new patient and review of the literatureC Rudin, L Thommen, C Fliegel, et al.
American Journal of Medical Genetics|August 26, 1998
Sibs affected with both Ehlers-Danlos syndrome type IV and cystic fibrosisA Jarisch, C Giunta, S Zielen, et al.
Tissue Antigens|September 1, 1994
Polylactosamine sugar chains expressed by epithelia of Henle's loop and collecting duct in rat and human kidney are selectively recognized by human cold agglutinins anti-I/iM Raghunath, C Grupp, I Neumann, et al.
The Biochemical Journal|December 15, 1987
Pyridinedicarboxylates, the first mechanism-derived inhibitors for prolyl 4-hydroxylase, selectively suppress cellular hydroxyprolyl biosynthesis. Decrease in interstitial collagen and Clq secretion in cell cultureG Tschank, M Raghunath, V Günzler, et al.
Zeitschrift Fur Kardiologie|May 20, 1998
[Marfan syndrome: diagnosis of cardiovascular manifestations]Y von Kodolitsch, M Raghunath, C Dieckmann, et al.
The Journal of Biological Chemistry|March 15, 1991
G to T transversion at position +5 of a splice donor site causes skipping of the preceding exon in the type III procollagen transcripts of a patient with Ehlers-Danlos syndrome type IVB Lee, E Vitale, A Superti-Furga, et al.
Helvetica Paediatrica Acta|January 1, 1979
Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathologyE R Baumgartner, H Wick, R Maurer, et al.
Archives of Biochemistry and Biophysics|October 15, 1983
Ascorbate deficiency results in decreased collagen production: under-hydroxylation of proline leads to increased intracellular degradationR A Berg, B Steinmann, S I Rennard, et al.
The Journal of Biological Chemistry|November 15, 1988
The structure of human collagen type IX and its organization in fetal and infant cartilage fibrilsP Bruckner, M Mendler, B Steinmann, et al.
The Journal of Investigative Dermatology|December 18, 1998
Transient bullous dermolysis of the newborn associated with compound heterozygosity for recessive and dominant COL7A1 mutationsN Hammami-Hauasli, M Raghunath, W Küster, et al.
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