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Molecular Genetics and Metabolism
|
February 9, 2020
The Undiagnosed Diseases Network International: Five years and more!
D Taruscio, G Baynam, H Cederroth, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 12, 2002
A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: data from the Italian Registry for Congenital Hypothyroidism (1991-1998)
A Olivieri, M A Stazi, P Mastroiacovo, et al.
European Journal of Medical Genetics
|
March 31, 2007
A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotype
F Berardinelli, A di Masi, M Salvatore, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
October 13, 2010
Characterization of HuH6, Hep3B, HepG2 and HLE liver cancer cell lines by WNT/β - catenin pathway, microRNA expression and protein expression profile
A Di Masi, M Viganotti, A Antoccia, et al.
The British Journal of Dermatology
|
November 12, 2009
Complex multipathways alterations and oxidative stress are associated with Hailey-Hailey disease
S Cialfi, C Oliviero, S Ceccarelli, et al.
Biomed Research International
|
March 14, 2013
The Italian National External quality assessment program in molecular genetic testing: results of the VII round (2010-2011)
F Censi, F Tosto, G Floridia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 13, 2018
Red Flags for early referral of people with symptoms suggestive of narcolepsy: a report from a national multidisciplinary panel
L Vignatelli, E Antelmi, I Ceretelli, et al.
Community Genetics
|
May 22, 2008
The Italian external quality assessment scheme in classical cytogenetics: four years of activity
G Floridia, V Falbo, F Censi, et al.
The European Journal of Health Economics : HEPAC : Health Economics in Prevention and Care
|
April 18, 2016
Social/economic costs and health-related quality of life in patients with juvenile idiopathic arthritis in Europe
A Kuhlmann, T Schmidt, M Treskova, et al.
Public Health Genomics
|
February 8, 2014
EUROPLAN: a project to support the development of national plans on rare diseases in Europe
D Taruscio, A E Gentile, M De Santis, et al.
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of 7
Search research articles
Search
Showing results (51-60 of 62) with videos related to
Sort By:
Page
of 7
Molecular Genetics and Metabolism
|
February 9, 2020
The Undiagnosed Diseases Network International: Five years and more!
D Taruscio, G Baynam, H Cederroth, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 12, 2002
A population-based study on the frequency of additional congenital malformations in infants with congenital hypothyroidism: data from the Italian Registry for Congenital Hypothyroidism (1991-1998)
A Olivieri, M A Stazi, P Mastroiacovo, et al.
European Journal of Medical Genetics
|
March 31, 2007
A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling "Nijmegen breakage syndrome" phenotype
F Berardinelli, A di Masi, M Salvatore, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)
|
October 13, 2010
Characterization of HuH6, Hep3B, HepG2 and HLE liver cancer cell lines by WNT/β - catenin pathway, microRNA expression and protein expression profile
A Di Masi, M Viganotti, A Antoccia, et al.
The British Journal of Dermatology
|
November 12, 2009
Complex multipathways alterations and oxidative stress are associated with Hailey-Hailey disease
S Cialfi, C Oliviero, S Ceccarelli, et al.
Biomed Research International
|
March 14, 2013
The Italian National External quality assessment program in molecular genetic testing: results of the VII round (2010-2011)
F Censi, F Tosto, G Floridia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 13, 2018
Red Flags for early referral of people with symptoms suggestive of narcolepsy: a report from a national multidisciplinary panel
L Vignatelli, E Antelmi, I Ceretelli, et al.
Community Genetics
|
May 22, 2008
The Italian external quality assessment scheme in classical cytogenetics: four years of activity
G Floridia, V Falbo, F Censi, et al.
The European Journal of Health Economics : HEPAC : Health Economics in Prevention and Care
|
April 18, 2016
Social/economic costs and health-related quality of life in patients with juvenile idiopathic arthritis in Europe
A Kuhlmann, T Schmidt, M Treskova, et al.
Public Health Genomics
|
February 8, 2014
EUROPLAN: a project to support the development of national plans on rare diseases in Europe
D Taruscio, A E Gentile, M De Santis, et al.
Page
of 7