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M Di Rocco

Showing results (31-40 of 115) with videos related to

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Minerva Pediatrica|April 30, 1981
[Therapeutic problems in the adrenogenital syndrome caused by salt-losing 21-hydroxylase deficiency. Appearance of signs of corticoid overdosage at normally used doses]A Iester, L Fasce, P Cambiaso, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1992
Point mutations in the tyrosine aminotransferase gene in tyrosinemia type IIE Natt, K Kida, M Odievre, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Neutropenia and impaired neutrophil function in glycogenosis type IbM Di Rocco, C Borrone, F Dallegri, et al.
Clinical Genetics|February 5, 2005
Winchester syndrome caused by a homozygous mutation affecting the active site of matrix metalloproteinase 2A Zankl, L Bonafé, V Calcaterra, et al.
European Journal of Histochemistry : EJH|January 1, 1997
Role of flow cytometric DNA analysis in the prognosis of endometrial carcinomaF Mangili, P De Marzi, M Di Rocco, et al.
AJNR. American Journal of Neuroradiology|March 13, 2009
MR imaging findings in 2 cases of late infantile GM1 gangliosidosisE De Grandis, M Di Rocco, A Pessagno, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 29, 2000
Outcome of thiamine treatment in a child with Leigh disease due to thiamine-responsive pyruvate dehydrogenase deficiencyM Di Rocco, L D Lamba, G Minniti, et al.
Journal of Medical Genetics|March 2, 1999
Ataxia, ocular telangiectasia, chromosome instability, and Langerhans cell histiocytosis in a patient with an unknown breakage syndromeM Di Rocco, A Arslanian, M Romanengo, et al.
Epilepsy Research|June 8, 2001
Malignant migrating partial seizures in infancyE Veneselli, M V Perrone, M Di Rocco, et al.
Minerva Pediatrica|October 31, 1984
[Pharmacologic and dietetic treatment of 2 siblings with atypical methylmalonic aciduria]M T Duillo, L Poggi, M Cortese, et al.
Pageof 12

Showing results (31-40 of 115) with videos related to

Sort By:
Pageof 12
Minerva Pediatrica|April 30, 1981
[Therapeutic problems in the adrenogenital syndrome caused by salt-losing 21-hydroxylase deficiency. Appearance of signs of corticoid overdosage at normally used doses]A Iester, L Fasce, P Cambiaso, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1992
Point mutations in the tyrosine aminotransferase gene in tyrosinemia type IIE Natt, K Kida, M Odievre, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Neutropenia and impaired neutrophil function in glycogenosis type IbM Di Rocco, C Borrone, F Dallegri, et al.
Clinical Genetics|February 5, 2005
Winchester syndrome caused by a homozygous mutation affecting the active site of matrix metalloproteinase 2A Zankl, L Bonafé, V Calcaterra, et al.
European Journal of Histochemistry : EJH|January 1, 1997
Role of flow cytometric DNA analysis in the prognosis of endometrial carcinomaF Mangili, P De Marzi, M Di Rocco, et al.
AJNR. American Journal of Neuroradiology|March 13, 2009
MR imaging findings in 2 cases of late infantile GM1 gangliosidosisE De Grandis, M Di Rocco, A Pessagno, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 29, 2000
Outcome of thiamine treatment in a child with Leigh disease due to thiamine-responsive pyruvate dehydrogenase deficiencyM Di Rocco, L D Lamba, G Minniti, et al.
Journal of Medical Genetics|March 2, 1999
Ataxia, ocular telangiectasia, chromosome instability, and Langerhans cell histiocytosis in a patient with an unknown breakage syndromeM Di Rocco, A Arslanian, M Romanengo, et al.
Epilepsy Research|June 8, 2001
Malignant migrating partial seizures in infancyE Veneselli, M V Perrone, M Di Rocco, et al.
Minerva Pediatrica|October 31, 1984
[Pharmacologic and dietetic treatment of 2 siblings with atypical methylmalonic aciduria]M T Duillo, L Poggi, M Cortese, et al.
Pageof 12