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Neurobiology of Aging
|
December 22, 2009
Effect of Coenzyme Q10 in mitigating oxidative DNA damage in Down syndrome patients, a double blind randomized controlled trial
L Tiano, P Carnevali, L Padella, et al.
International Journal of Immunopathology and Pharmacology
|
June 13, 2008
Effects of Holder pasteurization on human milk oligosaccharides
E Bertino, G V Coppa, F Giuliani, et al.
Metabolic Brain Disease
|
May 29, 2015
Mental retardation in mucopolysaccharidoses correlates with high molecular weight urinary heparan sulphate derived glucosamine
G V Coppa, O Gabrielli, L Zampini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1995
Bone marrow transplantation in Hunter syndrome (mucopolysaccharidosis type II): two-year follow-up of the first Italian patient and review of the literature
G V Coppa, O Gabrielli, L Zampini, et al.
Journal of Medical Genetics
|
August 16, 2003
Fabry disease: molecular studies in Italian patients and X inactivation analysis in manifesting carriers
A Morrone, C Cavicchi, T Bardelli, et al.
American Journal of Medical Genetics
|
September 1, 1990
Characterization of deletions in the dystrophin gene giving mild phenotypes
D R Love, T J Flint, R F Marsden, et al.
Minerva Pediatrica
|
October 1, 1996
The Williams syndrome: an Italian collaborative study
P Franceschini, A Guala, M P Vardeu, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
September 25, 2001
Prevalence and clinical picture of celiac disease in italian down syndrome patients: a multicenter study
M Bonamico, P Mariani, H M Danesi, et al.
American Journal of Human Genetics
|
February 11, 1999
Molecular analysis of SALL1 mutations in Townes-Brocks syndrome
J Kohlhase, P E Taschner, P Burfeind, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
June 27, 2001
[Registry of genetic and malformative diseases in the province of Macerata]
A Mercuri, O Amadori, A Andreozzi, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 70) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 70 results.
Neurobiology of Aging
|
December 22, 2009
Effect of Coenzyme Q10 in mitigating oxidative DNA damage in Down syndrome patients, a double blind randomized controlled trial
L Tiano, P Carnevali, L Padella, et al.
International Journal of Immunopathology and Pharmacology
|
June 13, 2008
Effects of Holder pasteurization on human milk oligosaccharides
E Bertino, G V Coppa, F Giuliani, et al.
Metabolic Brain Disease
|
May 29, 2015
Mental retardation in mucopolysaccharidoses correlates with high molecular weight urinary heparan sulphate derived glucosamine
G V Coppa, O Gabrielli, L Zampini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1995
Bone marrow transplantation in Hunter syndrome (mucopolysaccharidosis type II): two-year follow-up of the first Italian patient and review of the literature
G V Coppa, O Gabrielli, L Zampini, et al.
Journal of Medical Genetics
|
August 16, 2003
Fabry disease: molecular studies in Italian patients and X inactivation analysis in manifesting carriers
A Morrone, C Cavicchi, T Bardelli, et al.
American Journal of Medical Genetics
|
September 1, 1990
Characterization of deletions in the dystrophin gene giving mild phenotypes
D R Love, T J Flint, R F Marsden, et al.
Minerva Pediatrica
|
October 1, 1996
The Williams syndrome: an Italian collaborative study
P Franceschini, A Guala, M P Vardeu, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
September 25, 2001
Prevalence and clinical picture of celiac disease in italian down syndrome patients: a multicenter study
M Bonamico, P Mariani, H M Danesi, et al.
American Journal of Human Genetics
|
February 11, 1999
Molecular analysis of SALL1 mutations in Townes-Brocks syndrome
J Kohlhase, P E Taschner, P Burfeind, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
June 27, 2001
[Registry of genetic and malformative diseases in the province of Macerata]
A Mercuri, O Amadori, A Andreozzi, et al.
Page
of 7