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A Fiumara

Showing results (21-30 of 73) with videos related to

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Clinical Pediatrics|April 1, 1996
Multiple sclerosis with onset at 35 months of ageM Ruggieri, A Fiumara, L M Grimaldi, et al.
International Journal of Tissue Reactions|May 16, 2002
Assessment of skeletal status in patients with congenital disorder of glycosylation type IAR Barone, V Pavone, P Pennisi, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|June 1, 1990
Late-onset globoid cell leukodystrophy. Report on seven new patientsA Fiumara, L Pavone, L Siciliano, et al.
Journal of Inherited Metabolic Disease|December 23, 2006
Borderline mental development in a congenital disorder of glycosylation (CDG) type Ia patient with multisystemic involvement (intermediate phenotype)R Barone, L Sturiale, A Fiumara, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1987
[Neuronal ceroid lipofuscinosis. Description of a case]A Fiumara, G Nardone, F Nigro, et al.
Pediatric Neurology|October 6, 2001
Extraneurologic symptoms as presenting signs of Sanfilippo diseaseR Barone, A Fiumara, G R Villani, et al.
American Journal of Medical Genetics|May 3, 1996
Clinical and neuroradiological findings in classic infantile and late-onset globoid-cell leukodystrophy (Krabbe disease)R Barone, K Brühl, P Stoeter, et al.
Neuropediatrics|December 22, 1999
Clinical and neuroradiological follow-up in mucopolysaccharidosis type III (Sanfilippo syndrome)R Barone, F Nigro, F Triulzi, et al.
International Journal of Tissue Reactions|January 1, 1983
The effects of 2-(alpha-Tenoyl) thiopropionylglycine (TTPG) on human lung mucusM C Morale, A Fiumara, E Bousquet, et al.
Neuropediatrics|August 26, 2004
Epilepsy is not a prominent feature of primary autismP Pavone, G Incorpora, A Fiumara, et al.
Pageof 8

Showing results (21-30 of 73) with videos related to

Sort By:
Pageof 8
Clinical Pediatrics|April 1, 1996
Multiple sclerosis with onset at 35 months of ageM Ruggieri, A Fiumara, L M Grimaldi, et al.
International Journal of Tissue Reactions|May 16, 2002
Assessment of skeletal status in patients with congenital disorder of glycosylation type IAR Barone, V Pavone, P Pennisi, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|June 1, 1990
Late-onset globoid cell leukodystrophy. Report on seven new patientsA Fiumara, L Pavone, L Siciliano, et al.
Journal of Inherited Metabolic Disease|December 23, 2006
Borderline mental development in a congenital disorder of glycosylation (CDG) type Ia patient with multisystemic involvement (intermediate phenotype)R Barone, L Sturiale, A Fiumara, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1987
[Neuronal ceroid lipofuscinosis. Description of a case]A Fiumara, G Nardone, F Nigro, et al.
Pediatric Neurology|October 6, 2001
Extraneurologic symptoms as presenting signs of Sanfilippo diseaseR Barone, A Fiumara, G R Villani, et al.
American Journal of Medical Genetics|May 3, 1996
Clinical and neuroradiological findings in classic infantile and late-onset globoid-cell leukodystrophy (Krabbe disease)R Barone, K Brühl, P Stoeter, et al.
Neuropediatrics|December 22, 1999
Clinical and neuroradiological follow-up in mucopolysaccharidosis type III (Sanfilippo syndrome)R Barone, F Nigro, F Triulzi, et al.
International Journal of Tissue Reactions|January 1, 1983
The effects of 2-(alpha-Tenoyl) thiopropionylglycine (TTPG) on human lung mucusM C Morale, A Fiumara, E Bousquet, et al.
Neuropediatrics|August 26, 2004
Epilepsy is not a prominent feature of primary autismP Pavone, G Incorpora, A Fiumara, et al.
Pageof 8