Sfoglia per Autore
The fragile X in Sicily: an epidemiological survey
file da validare1988-01-01 Neri, G; Sanfilippo, S; Pavone, L; Mollica, F; Barberi, I; Giuffrè, L; Romano, C; Mattina, Teresa; Cammarata, M; Ragusa, Mg
Ichthyosis and neutral lipid storage disease
file da validare1988-01-01 Musumeci, S.; D(')Agata, A.; Romano, C.; Patane, R.; Cutrona, D.
Facial midline defect in the fetal alcohol syndrome. Embryogenetic considerations in two clinical cases
file da validare1988-01-01 Neri, G.; Sammito, V.; Romano, C.; Sanfilippo, S.; Opitz, J. M.; Reynolds, James F.
A Dermatoglyphic study of a group of Sicilian children with Fra-X syndrome
file da validare1988-01-01 Milone, G.; Conti, L.; Rizzo, Renata; Sanfilippo, S.; Sammito, V.; Romano, C.
FREQUENZA DELLE CONVULSIONI FEBBRILI NEI BAMBINI DOWN
file da validare1989-01-01 Romano, C; Tine', A; Fazio, G; Rizzo, Renata
FREQUENZA DELLE CONVULSIONI NEI BAMBINI DOWN
file da validare1989-01-01 Romano, C; Tine', A; Fazio, G; Rizzo, Renata
ARTROGRIPOSI MULTIPLA CONGENITA
file da validare1989-01-01 Rizzo, Renata; Innico, G; Romano, C.
Molecular analysis of aldolase B genes in hereditary fructose intolerance
file da validare1990-01-01 Cross, N. C. P.; Cox, T. M.; de Franchis, R.; Sebastio, G.; Dazzo, C.; Tolan, D. R.; Gregori, C.; Odievre, M.; Vidailhet, M.; Romano, V.; Mascali, G.; Romano, C.; Musumeci, S.; Steinmann, B.; Gitzelmann, R.
Low-Count Fragile-X Subjects in Fragile-X Positive Pedigrees: A Clinical and genetic Study of Two Families
file da validare1990-01-01 Romano, C; Barletta, C; Buono, Serafino; Ferri, R; Ragusa, Rm; Bergonzi, P.
Reliability of intradermal vaccination against HBV for accelerated prophylaxis
1990-01-01 Leonardi, Salvatore; Greco, D.; Sciacca, A.; Romano, C.; Musumeci, S.
Seizures in patients with trisomy 21
file da validare1990-01-01 Romano, C.; Tine', A.; Fazio, G.; Rizzo, Renata; Colognola, R. M.; Sorge, G.; Bergonzi, P.; Pavone, L.
Brain dysfunction and the immune system: lymphocyte's beta-adrenergic receptor in Down syndrome.
file da validare1990-01-01 Batticane, N; Morale, Mc; Romano, C; Cutuli, N; Marchetti, Bianca Maria
RFLP analysis in 5 Sicilian families with the fragile X syndrome
file da validare1991-01-01 Romano, V; Mascali, G; Chiavetta, V; Ragusa, Rm; Barletta, C; Romano, C; Mollica, F; Mattina, Teresa; Gross, A; Brown, Wt
Phenotypic and phoniatric findings in mosaic cri du chat syndrome
file da validare1991-01-01 Romano, C.; Ragusa, R. M.; Scillato, F.; Greco, D.; Amato, G.; Barletta, C.
Growth hormone subnormality in down syndrome [1]
file da validare1992-01-01 Ragusa, L.; Romano, C.; Failla, P.; Proto, C.; Colabucci, F.
Perforating Milia‐like Idiopathic Calcinosis Cutis and Periorbital Syringomas in a Girl With Down Syndrome
file da validare1994-01-01 Schepis, C.; Siragusa, M.; Palazzo, R.; Batolo, D.; Romano, C.
SKIN‐PICKING: THE BEST CUTANEOUS FEATURE IN THE RECOGNIZATION OF PRADER‐WILLI SYNDROME
file da validare1994-01-01 Schepis, C.; Failla, P.; Siragusa, M.; Romano, C.
A further family with epilepsy, dementia and yellow teeth: the Kohlschütter syndrome
file da validare1995-01-01 Musumeci, S. A.; Elia, M.; Ferri, R.; Romano, C.; Scuderi, C.; Del Gracco, S.
A CASE OF FG SYNDROME WITH GINGIVAL HYPERPLASIA AND KELOIDS
file da validare1995-01-01 Elia, M.; DI LELLO, R.; Romano, C.; Schepis, C.
Celiac disease in Down's syndrome with HLA serological and molecular studies
file da validare1996-01-01 Failla, P.; Ruberto, C.; Pagano, M. C.; Lombardo, M.; Bottaro, G.; Perichon, B.; Krishnamoorthy, R.; Romano, C.; Ragusa, A.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
The fragile X in Sicily: an epidemiological survey | 1-gen-1988 | Neri, G; Sanfilippo, S; Pavone, L; Mollica, F; Barberi, I; Giuffrè, L; Romano, C; Mattina, Teresa; Cammarata, M; Ragusa, Mg | file da validare |
Ichthyosis and neutral lipid storage disease | 1-gen-1988 | Musumeci, S.; D(')Agata, A.; Romano, C.; Patane, R.; Cutrona, D. | file da validare |
Facial midline defect in the fetal alcohol syndrome. Embryogenetic considerations in two clinical cases | 1-gen-1988 | Neri, G.; Sammito, V.; Romano, C.; Sanfilippo, S.; Opitz, J. M.; Reynolds, James F. | file da validare |
A Dermatoglyphic study of a group of Sicilian children with Fra-X syndrome | 1-gen-1988 | Milone, G.; Conti, L.; Rizzo, Renata; Sanfilippo, S.; Sammito, V.; Romano, C. | file da validare |
FREQUENZA DELLE CONVULSIONI FEBBRILI NEI BAMBINI DOWN | 1-gen-1989 | Romano, C; Tine', A; Fazio, G; Rizzo, Renata | file da validare |
FREQUENZA DELLE CONVULSIONI NEI BAMBINI DOWN | 1-gen-1989 | Romano, C; Tine', A; Fazio, G; Rizzo, Renata | file da validare |
ARTROGRIPOSI MULTIPLA CONGENITA | 1-gen-1989 | Rizzo, Renata; Innico, G; Romano, C. | file da validare |
Molecular analysis of aldolase B genes in hereditary fructose intolerance | 1-gen-1990 | Cross, N. C. P.; Cox, T. M.; de Franchis, R.; Sebastio, G.; Dazzo, C.; Tolan, D. R.; Gregori, C.; Odievre, M.; Vidailhet, M.; Romano, V.; Mascali, G.; Romano, C.; Musumeci, S.; Steinmann, B.; Gitzelmann, R. | file da validare |
Low-Count Fragile-X Subjects in Fragile-X Positive Pedigrees: A Clinical and genetic Study of Two Families | 1-gen-1990 | Romano, C; Barletta, C; Buono, Serafino; Ferri, R; Ragusa, Rm; Bergonzi, P. | file da validare |
Reliability of intradermal vaccination against HBV for accelerated prophylaxis | 1-gen-1990 | Leonardi, Salvatore; Greco, D.; Sciacca, A.; Romano, C.; Musumeci, S. | |
Seizures in patients with trisomy 21 | 1-gen-1990 | Romano, C.; Tine', A.; Fazio, G.; Rizzo, Renata; Colognola, R. M.; Sorge, G.; Bergonzi, P.; Pavone, L. | file da validare |
Brain dysfunction and the immune system: lymphocyte's beta-adrenergic receptor in Down syndrome. | 1-gen-1990 | Batticane, N; Morale, Mc; Romano, C; Cutuli, N; Marchetti, Bianca Maria | file da validare |
RFLP analysis in 5 Sicilian families with the fragile X syndrome | 1-gen-1991 | Romano, V; Mascali, G; Chiavetta, V; Ragusa, Rm; Barletta, C; Romano, C; Mollica, F; Mattina, Teresa; Gross, A; Brown, Wt | file da validare |
Phenotypic and phoniatric findings in mosaic cri du chat syndrome | 1-gen-1991 | Romano, C.; Ragusa, R. M.; Scillato, F.; Greco, D.; Amato, G.; Barletta, C. | file da validare |
Growth hormone subnormality in down syndrome [1] | 1-gen-1992 | Ragusa, L.; Romano, C.; Failla, P.; Proto, C.; Colabucci, F. | file da validare |
Perforating Milia‐like Idiopathic Calcinosis Cutis and Periorbital Syringomas in a Girl With Down Syndrome | 1-gen-1994 | Schepis, C.; Siragusa, M.; Palazzo, R.; Batolo, D.; Romano, C. | file da validare |
SKIN‐PICKING: THE BEST CUTANEOUS FEATURE IN THE RECOGNIZATION OF PRADER‐WILLI SYNDROME | 1-gen-1994 | Schepis, C.; Failla, P.; Siragusa, M.; Romano, C. | file da validare |
A further family with epilepsy, dementia and yellow teeth: the Kohlschütter syndrome | 1-gen-1995 | Musumeci, S. A.; Elia, M.; Ferri, R.; Romano, C.; Scuderi, C.; Del Gracco, S. | file da validare |
A CASE OF FG SYNDROME WITH GINGIVAL HYPERPLASIA AND KELOIDS | 1-gen-1995 | Elia, M.; DI LELLO, R.; Romano, C.; Schepis, C. | file da validare |
Celiac disease in Down's syndrome with HLA serological and molecular studies | 1-gen-1996 | Failla, P.; Ruberto, C.; Pagano, M. C.; Lombardo, M.; Bottaro, G.; Perichon, B.; Krishnamoorthy, R.; Romano, C.; Ragusa, A. | file da validare |
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