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L Pavone

Showing results (141-150 of 165) with videos related to

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Neuropediatrics|August 28, 2010
Neurological manifestations in individuals with pure cutaneous or syndromic (Ruggieri-Happle syndrome) phenotypes with "cutis tricolor": a study of 14 casesE Lionetti, P Pavone, I Kennerknecht, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Lysosomal enzyme activities in serum and leukocytes from patients with carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase deficiency)R Barone, H Carchon, E Jansen, et al.
Brain & Development|January 1, 1989
Late febrile convulsions: a clinical follow-upL Pavone, G B Cavazzuti, G Incorpora, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Seizures in patients with trisomy 21C Romano, A Tiné, G Fazio, et al.
Journal of Medical Genetics|March 1, 1997
Tuberous sclerosis complex: neonatal deaths in three of four children of consanguineous, non-expressing parentsM Ruggieri, C Carbonara, G Magro, et al.
International Journal of Immunopathology and Pharmacology|June 16, 2012
Acquired peripheral neuropathy: a report on 20 childrenP Pavone, A D Praticò, M Ruggieri, et al.
Cancer|December 18, 2001
Long-term immunotherapy with low-dose interleukin-2 and interferon-alpha in the treatment of patients with advanced renal cell carcinomaC Buzio, S Andrulli, R Santi, et al.
Muscle & Nerve|March 1, 1980
Autosomal recessive generalized myotoniaH Zellweger, L Pavone, A Biondi, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMDTh Voit, E Parano, V Straub, et al.
Neurology|February 1, 1991
Epidermal nevus syndrome: a neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures, and facial hemihypertrophyL Pavone, P Curatolo, R Rizzo, et al.
Pageof 17

Showing results (141-150 of 165) with videos related to

Sort By:
Pageof 17
Neuropediatrics|August 28, 2010
Neurological manifestations in individuals with pure cutaneous or syndromic (Ruggieri-Happle syndrome) phenotypes with "cutis tricolor": a study of 14 casesE Lionetti, P Pavone, I Kennerknecht, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Lysosomal enzyme activities in serum and leukocytes from patients with carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase deficiency)R Barone, H Carchon, E Jansen, et al.
Brain & Development|January 1, 1989
Late febrile convulsions: a clinical follow-upL Pavone, G B Cavazzuti, G Incorpora, et al.
American Journal of Medical Genetics. Supplement|January 1, 1990
Seizures in patients with trisomy 21C Romano, A Tiné, G Fazio, et al.
Journal of Medical Genetics|March 1, 1997
Tuberous sclerosis complex: neonatal deaths in three of four children of consanguineous, non-expressing parentsM Ruggieri, C Carbonara, G Magro, et al.
International Journal of Immunopathology and Pharmacology|June 16, 2012
Acquired peripheral neuropathy: a report on 20 childrenP Pavone, A D Praticò, M Ruggieri, et al.
Cancer|December 18, 2001
Long-term immunotherapy with low-dose interleukin-2 and interferon-alpha in the treatment of patients with advanced renal cell carcinomaC Buzio, S Andrulli, R Santi, et al.
Muscle & Nerve|March 1, 1980
Autosomal recessive generalized myotoniaH Zellweger, L Pavone, A Biondi, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMDTh Voit, E Parano, V Straub, et al.
Neurology|February 1, 1991
Epidermal nevus syndrome: a neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures, and facial hemihypertrophyL Pavone, P Curatolo, R Rizzo, et al.
Pageof 17