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Thrombosis and Haemostasis
|
October 1, 1996
Haemostatic studies in carbohydrate-deficient glycoprotein syndrome type I
A Fiumara, R Barone, P Buttitta, et al.
Pediatric Neurology
|
October 8, 1999
Peripheral lymphocyte subsets and other immune aspects in Rett syndrome
A Fiumara, A Sciotto, R Barone, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
First-trimester prenatal diagnosis of Canavan disease
M O Rolland, P Divry, G Mandon, et al.
Clinical Genetics
|
April 1, 1995
Inter- and intrafamilial variability in mucolipidosis II (I-cell disease)
M Beck, R Barone, R Hoffmann, et al.
Pediatric Neurology
|
September 1, 1995
Congenital muscular dystrophies: clinical review and proposed classification
E Parano, L Pavone, A Fiumara, et al.
Clinical Genetics
|
November 13, 2010
Krabbe leukodystrophy in a selected population with high rate of late onset forms: longer survival linked to c.121G>A (p.Gly41Ser) mutation
A Fiumara, R Barone, A Arena, et al.
American Journal of Medical Genetics
|
June 27, 1997
Two new mild homozygous mutations in Gaucher disease patients: clinical signs and biochemical analyses
B Cormand, D Grinberg, L Gort, et al.
Journal of Endocrinological Investigation
|
December 1, 1995
Early occurrence of a thyroid carcinoma in a patient who developed Graves' disease after treatment for Hodgkin's disease
A Belfiore, G Pellegriti, G Milone, et al.
Muscle & Nerve
|
June 1, 1994
Immunocytochemistry of muscle cytoskeletal proteins in acid maltase deficiency
G Vita, A Migliorato, A Toscano, et al.
Journal of Neurology
|
October 1, 1996
Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type I
L Pavone, A Fiumara, R Barone, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 73) with videos related to
Sort By:
Page
of 8
Thrombosis and Haemostasis
|
October 1, 1996
Haemostatic studies in carbohydrate-deficient glycoprotein syndrome type I
A Fiumara, R Barone, P Buttitta, et al.
Pediatric Neurology
|
October 8, 1999
Peripheral lymphocyte subsets and other immune aspects in Rett syndrome
A Fiumara, A Sciotto, R Barone, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
First-trimester prenatal diagnosis of Canavan disease
M O Rolland, P Divry, G Mandon, et al.
Clinical Genetics
|
April 1, 1995
Inter- and intrafamilial variability in mucolipidosis II (I-cell disease)
M Beck, R Barone, R Hoffmann, et al.
Pediatric Neurology
|
September 1, 1995
Congenital muscular dystrophies: clinical review and proposed classification
E Parano, L Pavone, A Fiumara, et al.
Clinical Genetics
|
November 13, 2010
Krabbe leukodystrophy in a selected population with high rate of late onset forms: longer survival linked to c.121G>A (p.Gly41Ser) mutation
A Fiumara, R Barone, A Arena, et al.
American Journal of Medical Genetics
|
June 27, 1997
Two new mild homozygous mutations in Gaucher disease patients: clinical signs and biochemical analyses
B Cormand, D Grinberg, L Gort, et al.
Journal of Endocrinological Investigation
|
December 1, 1995
Early occurrence of a thyroid carcinoma in a patient who developed Graves' disease after treatment for Hodgkin's disease
A Belfiore, G Pellegriti, G Milone, et al.
Muscle & Nerve
|
June 1, 1994
Immunocytochemistry of muscle cytoskeletal proteins in acid maltase deficiency
G Vita, A Migliorato, A Toscano, et al.
Journal of Neurology
|
October 1, 1996
Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type I
L Pavone, A Fiumara, R Barone, et al.
Page
of 8