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Helvetica Paediatrica Acta|November 1, 1978
Hyperornithinemia and gyrate atrophy of choroid and retina. Report of a caseG Stoppoloni, F Prisco, R Santinelli, et al.
Pediatric Nephrology (Berlin, Germany)|December 1, 1995
Concealed administration of frusemide simulating Bartter syndrome in a 4.5-year-old boyM D'Avanzo, R Santinelli, C Tolone, et al.
Nephron|January 1, 1978
Lysine in treatment of hyperornithinemiaC Giordano, N G De Santo, M Pluvio, et al.
Archives of Neurology|June 17, 1998
Familial idiopathic intracranial hypertension with spinal and radicular painR Santinelli, C Tolone, R Toraldo, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1992
Macroamylasemia in a 5-year-old girlM D'Avanzo, C Cobbaert, C Tolone, et al.
Pediatric Hematology and Oncology|March 1, 1994
Heterogeneity of the erythropoietic defect in two cases of Aase-Smith syndromeM D'Avanzo, V Pistoia, R Santinelli, et al.
Journal of Inherited Metabolic Disease|May 26, 2004
Low-protein diet and progression of retinal degeneration in gyrate atrophy of the choroid and retina: a twenty-six-year follow-upR Santinelli, C Costagliola, C Tolone, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1986
[Unusual course of a case of urethral rhabdomyosarcoma in a 10-year-old boy]M D'Avanzo, A Savanelli, C Tolone, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|April 23, 2003
Late onset Blueberry Muffin Syndrome following congenital rubellaA Vozza, C Tolone, E M Carrano, et al.
Physical Review Letters|April 3, 2012
Search for lepton number violating decays B+ → π- μ+ μ+ and B+ → K- μ+ μ+R Aaij, C Abellan Beteta, B Adeva, et al.
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