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M Di Rocco

Showing results (11-20 of 115) with videos related to

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Clinical Genetics|October 23, 1997
Rhombencephalosynapsis with facial anomalies and probable autosomal recessive inheritance: a case reportM Romanengo, P Tortori-Donati, M Di Rocco
Journal of Inherited Metabolic Disease|January 1, 1985
An abnormal amino acid pattern in adenosine deaminase deficiencyC Borrone, M Di Rocco, U Caruso, et al.
Pediatric Radiology|January 1, 1993
Sponastrime dysplasia: report on two siblings with metal retardationG Camera, A Camera, M Di Rocco, et al.
Annals of the Rheumatic Diseases|September 6, 2001
Non-steroidal anti-inflammatory drugs in the treatment of hyper-IgD syndromeP Picco, M Gattorno, M Di Rocco, et al.
European Journal of Pediatrics|June 1, 1991
Intracranial calcifications and nephrogenic diabetes insipidusM Di Rocco, P Picco, P Gandullia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
Neurophysiological findings in a case of carbohydrate-deficient glycoprotein (CDG) syndrome type I with phosphomannomutase deficiencyE Veneselli, R Biancheri, M Di Rocco, et al.
Journal of Computer Assisted Tomography|March 1, 1989
Leigh disease: value of CT in presymptomatic patients and variability of the lesions with timeA Taccone, M Di Rocco, P Fondelli, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
De novo 13q31.1-q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2E Tassano, M Di Rocco, S Signa, et al.
European Journal of Pediatrics|September 1, 2000
Osteopetrorickets: case reportM Di Rocco, A Buoncompagni, A Loy, et al.
American Journal of Medical Genetics|July 19, 2002
Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: further case of Hennekam syndrome with a severe phenotypeF Forzano, F Faravelli, A Loy, et al.
Pageof 12

Showing results (11-20 of 115) with videos related to

Sort By:
Pageof 12
Clinical Genetics|October 23, 1997
Rhombencephalosynapsis with facial anomalies and probable autosomal recessive inheritance: a case reportM Romanengo, P Tortori-Donati, M Di Rocco
Journal of Inherited Metabolic Disease|January 1, 1985
An abnormal amino acid pattern in adenosine deaminase deficiencyC Borrone, M Di Rocco, U Caruso, et al.
Pediatric Radiology|January 1, 1993
Sponastrime dysplasia: report on two siblings with metal retardationG Camera, A Camera, M Di Rocco, et al.
Annals of the Rheumatic Diseases|September 6, 2001
Non-steroidal anti-inflammatory drugs in the treatment of hyper-IgD syndromeP Picco, M Gattorno, M Di Rocco, et al.
European Journal of Pediatrics|June 1, 1991
Intracranial calcifications and nephrogenic diabetes insipidusM Di Rocco, P Picco, P Gandullia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
Neurophysiological findings in a case of carbohydrate-deficient glycoprotein (CDG) syndrome type I with phosphomannomutase deficiencyE Veneselli, R Biancheri, M Di Rocco, et al.
Journal of Computer Assisted Tomography|March 1, 1989
Leigh disease: value of CT in presymptomatic patients and variability of the lesions with timeA Taccone, M Di Rocco, P Fondelli, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
De novo 13q31.1-q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2E Tassano, M Di Rocco, S Signa, et al.
European Journal of Pediatrics|September 1, 2000
Osteopetrorickets: case reportM Di Rocco, A Buoncompagni, A Loy, et al.
American Journal of Medical Genetics|July 19, 2002
Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: further case of Hennekam syndrome with a severe phenotypeF Forzano, F Faravelli, A Loy, et al.
Pageof 12