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Annales De Pediatrie|February 1, 1990
[Nail-patella syndrome without extra-renal lesions. A new hereditary glomerular nephropathy]M C Gubler, J P Dommergues, J Furioli, et al.Endoscopy|May 7, 2009
Is there an advantage to be gained from adding digital image cytometry of brush cytology to a standard biopsy protocol in patients with Barrett's esophagus?J Borovicka, R Schönegg, M Hell, et al.Endoscopy|September 1, 2010
Air suctioning during colon biopsy forceps removal reduces bacterial air contamination in the endoscopy suiteS R Vavricka, R Tutuian, A Imhof, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 28, 2021
Pathological and sonographic review of early isolated severe lower urinary tract obstruction and implications for prenatal treatmentN Vinit, B Bessières, E Spaggiari, et al.Genomics|December 10, 1995
A 11 Mb YAC-based contig spanning the familial juvenile nephronophthisis region (NPH1) located on chromosome 2qM Konrad, S Saunier, F Silbermann, et al.Nature Genetics|March 31, 2000
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndromeN Boute, O Gribouval, S Roselli, et al.Nephron|January 1, 1982
A new form of familial glomerulonephritisO Kourilsky, M C Gubler, L Morel-Maroger, et al.American Journal of Human Genetics|July 1, 1992
Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-amplified lymphoblast cDNA fragmentsB Knebelmann, G Deschenes, F Gros, et al.Human Molecular Genetics|March 1, 1996
Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisisM Konrad, S Saunier, L Heidet, et al.Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 15, 2001
Congenital erythropoietic porphyria: prenatal diagnosis and autopsy findings in two sibling fetusesF Daïkha-Dahmane, M Dommergues, F Narcy, et al.Pageof 23