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Pediatric Nephrology (Berlin, Germany)|April 1, 1996
Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish populationA Fuchshuber, P Niaudet, O Gribouval, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1985
[Diffuse arterial calcified elastopathy]C Antignac, M C Gubler, L Garel, et al.European Journal of Ophthalmology|July 9, 2008
Bilateral macular detachment caused by bilateral optic nerve malformation in a papillorenal syndrome due to a new PAX2 mutationS Samimi, C Antignac, C Combe, et al.Mathematical Biosciences|January 23, 2010
Activity pattern detection in electroneurographic and electromyogram signals through a heteroscedastic change-point methodM E Esquivel-Frausto, J A Guerrero, J E Macías-DíazCureus|August 5, 2024
Adrenocorticotropic Hormone Producing Pituitary Carcinoma in the Falx Cerebri, Retroclival Region, Ethmoidal Cells, and Other LocationsJose E Esquivel, Ana B Santos, Anthony Hong, et al.Experimental Brain Research|March 22, 2020
Modulation of ellipses drawing by sonificationEric O Boyer, Frederic Bevilacqua, Emmanuel Guigon, et al.Journal of Pediatric Urology|September 4, 2019
Left lateral retroperitoneoscopic total nephrectomy of a horseshoe kidney in a 3-year-old boyH Lottmann, L Pio, Y Heloury, et al.Human Molecular Genetics|April 1, 1995
Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndromeB Knebelmann, L Forestier, L Drouot, et al.Gastroenterology|February 24, 2001
Diffuse esophageal leiomyomatosis with perirectal involvement mimicking Hirschsprung diseaseP Guillem, F Delcambre, L Cohen-Solal, et al.American Journal of Medical Genetics|May 30, 1998
Medullary cystic kidney disease with hyperuricemia and gout in a large Cypriot family: no allelism with nephronophthisis type 1C Stavrou, A Pierides, I Zouvani, et al.Pageof 16