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Journal of Submicroscopic Cytology and Pathology
|
May 7, 2002
Nemaline myopathy: description of an adult onset case
F Ginanneschi, M Mondelli, A Malandrini, et al.
Journal of Neurology
|
January 11, 2001
Heteroplasmy of the A3243G transition of mitochondrial tRNA(Leu(UUR)) in a MELAS case and in a 25-week-old miscarried fetus
E Cardaioli, G M Fabrizi, G S Grieco, et al.
American Journal of Medical Genetics. Part A
|
September 5, 2003
Retinochoroidal atrophy in two adult patients with Angelman syndrome
A Rufa, M T Dotti, A Orrico, et al.
Journal of the Neurological Sciences
|
August 14, 1998
Giant axonal neuropathy with subclinical involvement of the central nervous system: case report
A Malandrini, M T Dotti, C Battisti, et al.
Acta Neurologica
|
October 1, 1986
Familial multiple exostoses syndrome: a phacomatosis of bone tissue
N Volpi, M T Dotti, F Giannini, et al.
Journal of Lipid Research
|
October 1, 1996
Urinary excretion of mevalonic acid as an indicator of cholesterol synthesis
B Lindenthal, A Simatupang, M T Dotti, et al.
Acta Neurologica
|
June 1, 1987
Adrenoleukodystrophy: a genetic, clinical, biochemical and computed tomographic study of four patients in three different families
M T Dotti, P Annunziata, I D'Amore, et al.
American Journal of Medical Genetics
|
February 5, 1998
Schnyder corneal crystalline dystrophy: description of a new family with evidence of abnormal lipid storage in skin fibroblasts
C Battisti, M T Dotti, A Malandrini, et al.
Brain & Development
|
March 1, 1993
Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical study
M T Dotti, L Manneschi, A Malandrini, et al.
Human Genetics
|
April 4, 2008
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL
Silvia Bianchi, M T Dotti, A Perretti, et al.
Page
of 15
Search research articles
Search
Showing results (51-60 of 144) with videos related to
Sort By:
Page
of 15
Journal of Submicroscopic Cytology and Pathology
|
May 7, 2002
Nemaline myopathy: description of an adult onset case
F Ginanneschi, M Mondelli, A Malandrini, et al.
Journal of Neurology
|
January 11, 2001
Heteroplasmy of the A3243G transition of mitochondrial tRNA(Leu(UUR)) in a MELAS case and in a 25-week-old miscarried fetus
E Cardaioli, G M Fabrizi, G S Grieco, et al.
American Journal of Medical Genetics. Part A
|
September 5, 2003
Retinochoroidal atrophy in two adult patients with Angelman syndrome
A Rufa, M T Dotti, A Orrico, et al.
Journal of the Neurological Sciences
|
August 14, 1998
Giant axonal neuropathy with subclinical involvement of the central nervous system: case report
A Malandrini, M T Dotti, C Battisti, et al.
Acta Neurologica
|
October 1, 1986
Familial multiple exostoses syndrome: a phacomatosis of bone tissue
N Volpi, M T Dotti, F Giannini, et al.
Journal of Lipid Research
|
October 1, 1996
Urinary excretion of mevalonic acid as an indicator of cholesterol synthesis
B Lindenthal, A Simatupang, M T Dotti, et al.
Acta Neurologica
|
June 1, 1987
Adrenoleukodystrophy: a genetic, clinical, biochemical and computed tomographic study of four patients in three different families
M T Dotti, P Annunziata, I D'Amore, et al.
American Journal of Medical Genetics
|
February 5, 1998
Schnyder corneal crystalline dystrophy: description of a new family with evidence of abnormal lipid storage in skin fibroblasts
C Battisti, M T Dotti, A Malandrini, et al.
Brain & Development
|
March 1, 1993
Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical study
M T Dotti, L Manneschi, A Malandrini, et al.
Human Genetics
|
April 4, 2008
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL
Silvia Bianchi, M T Dotti, A Perretti, et al.
Page
of 15