Sfoglia per Autore
Adrenoleukodystrophy. Validity of CT in the diagnosis.
file da validare1982-01-01 Pavone, L; Pero, G; Fiumara, Agata; La Rosa, M; Scialfa, G.
The effects of 2-(alpha-Tenoyl) thiopropionylglycine (TTPG) on human lung mucus.
file da validare1983-01-01 Morale, Mc; Fiumara, Agata; Bousquet, E; Matera, M; Guarcello, V; Rizza, V.
Determination of C20-C30 fatty acids by reversed-phase chromatographic techniques: an efficient method to quantitate minor fatty acids in serum of patients with adrenoleukodystrophy.
file da validare1984-01-01 Alberghina, M; Fiumara, Agata; Pavone, L; Giuffrida, A. M.
Effects of carnitine and acetylcarnitine isomers on mitochondrial respiration.
file da validare1984-01-01 Farinella, Z; Fiumara, Agata; Bianciardi, P; Guarcello, V; Rizza, V.
Late-onset globoid cell leukodystrophy. Report on seven new patients.
file da validare1985-01-01 Fiumara, Agata; Pavone, L; Siciliano, L; Tinè, A; Parano, E; Innico, G.
Ittiosi lamellare congenita in 2 sorelle affette da aminoglicinuria, follow-up di 8 anni
file da validare1985-01-01 Fiumara, Agata; S., Garozzo; C., Micale; Micali, Giuseppe; C., Meli
Niemann-Pick disease type B: clinical signs and follow-up of a new case.Niemann-Pick disease type B: clinical signs and follow-up of a new case.
file da validare1986-01-01 Pavone, L; Fiumara, Agata; Larosa, M.
Neuronal ceroid lipofuscinosis. Description of a case. Pediatr Med Chir. 1987 Nov-Dec;9(6):757-60. Italian. PMID: 3444750
file da validare1987-01-01 Fiumara, Agata; Nardone, G; Nigro, F; Meli, C; Siciliano, L; Gullotta, F.
VARIABILITA'CLINICA DELLA SINDROME DI BECKWITH - WIEDEMAN. PRESENTAZIONE DI OTTO PAZIENTI
file da validare1988-01-01 Sorge, G; DI FORTI, F; Fiumara, Agata; Garozzo, R; Rizzo, Renata
PARTIAL LIPODYSTROPHY - IMMUNOLOGICAL STUDIES IN A SICILIAN GIRL
file da validare1989-01-01 Fiumara, Agata; Mazzarino, Maria Clorinda; Distefano, Va; Micali, G; Mancuso, Gr; Larosa, M.
Partial lipodystrophy: immunologic studies in a Sicilian girl.
file da validare1989-01-01 Fiumara, Agata; Mazzarino, Mc; Di Stefano, Va; Micali, G; Mancuso, Gr; PMID: 2919800, La Rosa M.
On a rare atypical form of metachromatic leukodystrophy (MLD): "neurological non-mld patients with low levels of arylsulphatase A". Description of two cases.
file da validare1989-01-01 Grasso, A; Fiumara, Agata; Biondi, R; Nigro, F; Nardone, G; Bonomo, Mg; Sicurella, L; Scrofani, A.
Late-onset globoid cell leukodystrophy. Report on seven new patients.
file da validare1990-01-01 Fiumara, Agata; Pavone, L; Siciliano, L; Tinè, A; Parano, E; Innico, G.
Patient with multiple congenital anomalies and decreased production and processing of procollagen in cultured fibroblasts.
file da validare1991-01-01 Pavone, L; Incorpora, G; Fiumara, Agata; Sorge, G; Ramirez, F; Mcgarry, J; Wootten, J; Minor, R.
GLYCOGENOSIS THE AUTHOR'S EXPERIENCE WITH POMPE DISEASE
file da validare1991-01-01 Fiumara, Agata
Plasma β-endorphin levels and natural killer cells in two cases of congenital indifference to pain
file da validare1992-01-01 Bernardini, Renato; Tine, A; Mauceri, G; Mazzarino, Mc; Malaponte, G; Nicosia, A; Parano, E; Fiumara, Agata
Sanfilippo syndrome type D in two adolescent sisters.
file da validare1992-01-01 Siciliano, L; Fiumara, Agata; Pavone, L; Freeman, C; Robertson, D; Morris, Cp; Hopwood, Jj; Di Natale, P; Musumeci, S; Horwitz, A. L.
Carbohydrate deficient Glycoprotein Syndrome: Report on two new cases.
file da validare1993-01-01 L., Pavone; Rizzo, Renata; Barone, RITA MARIA ELISA; Fiumara, Agata; J., Jaeken
Syndactyly type II with cataract and mental retardation
file da validare1993-01-01 L., Pavone; Fiumara, Agata; Rizzo, Renata; E., Parano; G., Incorpora
First-trimester prenatal diagnosis of Canavan disease.
file da validare1993-01-01 Rolland, Mo; Divry, P; Mandon, G; Thoulon, Jm; Fiumara, Agata; Mathieu, M.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Adrenoleukodystrophy. Validity of CT in the diagnosis. | 1-gen-1982 | Pavone, L; Pero, G; Fiumara, Agata; La Rosa, M; Scialfa, G. | file da validare |
The effects of 2-(alpha-Tenoyl) thiopropionylglycine (TTPG) on human lung mucus. | 1-gen-1983 | Morale, Mc; Fiumara, Agata; Bousquet, E; Matera, M; Guarcello, V; Rizza, V. | file da validare |
Determination of C20-C30 fatty acids by reversed-phase chromatographic techniques: an efficient method to quantitate minor fatty acids in serum of patients with adrenoleukodystrophy. | 1-gen-1984 | Alberghina, M; Fiumara, Agata; Pavone, L; Giuffrida, A. M. | file da validare |
Effects of carnitine and acetylcarnitine isomers on mitochondrial respiration. | 1-gen-1984 | Farinella, Z; Fiumara, Agata; Bianciardi, P; Guarcello, V; Rizza, V. | file da validare |
Late-onset globoid cell leukodystrophy. Report on seven new patients. | 1-gen-1985 | Fiumara, Agata; Pavone, L; Siciliano, L; Tinè, A; Parano, E; Innico, G. | file da validare |
Ittiosi lamellare congenita in 2 sorelle affette da aminoglicinuria, follow-up di 8 anni | 1-gen-1985 | Fiumara, Agata; S., Garozzo; C., Micale; Micali, Giuseppe; C., Meli | file da validare |
Niemann-Pick disease type B: clinical signs and follow-up of a new case.Niemann-Pick disease type B: clinical signs and follow-up of a new case. | 1-gen-1986 | Pavone, L; Fiumara, Agata; Larosa, M. | file da validare |
Neuronal ceroid lipofuscinosis. Description of a case. Pediatr Med Chir. 1987 Nov-Dec;9(6):757-60. Italian. PMID: 3444750 | 1-gen-1987 | Fiumara, Agata; Nardone, G; Nigro, F; Meli, C; Siciliano, L; Gullotta, F. | file da validare |
VARIABILITA'CLINICA DELLA SINDROME DI BECKWITH - WIEDEMAN. PRESENTAZIONE DI OTTO PAZIENTI | 1-gen-1988 | Sorge, G; DI FORTI, F; Fiumara, Agata; Garozzo, R; Rizzo, Renata | file da validare |
PARTIAL LIPODYSTROPHY - IMMUNOLOGICAL STUDIES IN A SICILIAN GIRL | 1-gen-1989 | Fiumara, Agata; Mazzarino, Maria Clorinda; Distefano, Va; Micali, G; Mancuso, Gr; Larosa, M. | file da validare |
Partial lipodystrophy: immunologic studies in a Sicilian girl. | 1-gen-1989 | Fiumara, Agata; Mazzarino, Mc; Di Stefano, Va; Micali, G; Mancuso, Gr; PMID: 2919800, La Rosa M. | file da validare |
On a rare atypical form of metachromatic leukodystrophy (MLD): "neurological non-mld patients with low levels of arylsulphatase A". Description of two cases. | 1-gen-1989 | Grasso, A; Fiumara, Agata; Biondi, R; Nigro, F; Nardone, G; Bonomo, Mg; Sicurella, L; Scrofani, A. | file da validare |
Late-onset globoid cell leukodystrophy. Report on seven new patients. | 1-gen-1990 | Fiumara, Agata; Pavone, L; Siciliano, L; Tinè, A; Parano, E; Innico, G. | file da validare |
Patient with multiple congenital anomalies and decreased production and processing of procollagen in cultured fibroblasts. | 1-gen-1991 | Pavone, L; Incorpora, G; Fiumara, Agata; Sorge, G; Ramirez, F; Mcgarry, J; Wootten, J; Minor, R. | file da validare |
GLYCOGENOSIS THE AUTHOR'S EXPERIENCE WITH POMPE DISEASE | 1-gen-1991 | Fiumara, Agata | file da validare |
Plasma β-endorphin levels and natural killer cells in two cases of congenital indifference to pain | 1-gen-1992 | Bernardini, Renato; Tine, A; Mauceri, G; Mazzarino, Mc; Malaponte, G; Nicosia, A; Parano, E; Fiumara, Agata | file da validare |
Sanfilippo syndrome type D in two adolescent sisters. | 1-gen-1992 | Siciliano, L; Fiumara, Agata; Pavone, L; Freeman, C; Robertson, D; Morris, Cp; Hopwood, Jj; Di Natale, P; Musumeci, S; Horwitz, A. L. | file da validare |
Carbohydrate deficient Glycoprotein Syndrome: Report on two new cases. | 1-gen-1993 | L., Pavone; Rizzo, Renata; Barone, RITA MARIA ELISA; Fiumara, Agata; J., Jaeken | file da validare |
Syndactyly type II with cataract and mental retardation | 1-gen-1993 | L., Pavone; Fiumara, Agata; Rizzo, Renata; E., Parano; G., Incorpora | file da validare |
First-trimester prenatal diagnosis of Canavan disease. | 1-gen-1993 | Rolland, Mo; Divry, P; Mandon, G; Thoulon, Jm; Fiumara, Agata; Mathieu, M. | file da validare |
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