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Clinical Genetics
|
January 23, 2010
Eyebrow anomalies as a diagnostic sign of genomic disorders
M Silengo, E Belligni, C Molinatto, et al.
Minerva Pediatrica
|
April 14, 2011
A child with macrocephaly: case report of a patient with megalencephalic leukoencephalopathy with subcortical cysts and a compound heterozygosity for two mutations in the MLC1 gene
A G Delmonaco, E Gaidolfi, G C Scheper, et al.
American Journal of Medical Genetics
|
January 15, 1994
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization
E A Lindsay, A Grillo, G B Ferrero, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
July 1, 1996
Long term recombinant interferon alpha treatment in MS with special emphasis to side effects
L Durelli, M R Bongioanni, B Ferrero, et al.
Revista Espanola De Oncologia
|
January 1, 1984
Intrathecal opiates for chronic pain in cancer patients
A González Navarro, H M Zimman Mansfeld, T Molinero Aparicio, et al.
Frontiers in Pediatrics
|
May 4, 2023
Case report: Gastroenterological management in a case of cardio-facio-cutaneous syndrome
B Ciacchini, G Di Nardo, M Marin, et al.
Journal of Medical Genetics
|
May 19, 2001
Suggestive linkage of situs inversus and other left-right axis anomalies to chromosome 6p
E Vitale, V Brancolini, A De Rienzo, et al.
American Journal of Human Genetics
|
August 1, 1997
A submicroscopic deletion in Xq26 associated with familial situs ambiguus
G B Ferrero, M Gebbia, G Pilia, et al.
Expert Opinion on Biological Therapy
|
March 13, 2009
Neutralizing antibodies in multiple sclerosis patients treated with 375 micrograms interferon-beta-1b
L Durelli, P Barbero, A Cucci, et al.
Autoimmunity Reviews
|
August 16, 2008
Anti-neuronal antibodies in patients with HCV-related mixed cryoglobulinemia
M Alpa, B Ferrero, R Cavallo, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 97) with videos related to
Sort By:
Page
of 10
Clinical Genetics
|
January 23, 2010
Eyebrow anomalies as a diagnostic sign of genomic disorders
M Silengo, E Belligni, C Molinatto, et al.
Minerva Pediatrica
|
April 14, 2011
A child with macrocephaly: case report of a patient with megalencephalic leukoencephalopathy with subcortical cysts and a compound heterozygosity for two mutations in the MLC1 gene
A G Delmonaco, E Gaidolfi, G C Scheper, et al.
American Journal of Medical Genetics
|
January 15, 1994
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization
E A Lindsay, A Grillo, G B Ferrero, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
July 1, 1996
Long term recombinant interferon alpha treatment in MS with special emphasis to side effects
L Durelli, M R Bongioanni, B Ferrero, et al.
Revista Espanola De Oncologia
|
January 1, 1984
Intrathecal opiates for chronic pain in cancer patients
A González Navarro, H M Zimman Mansfeld, T Molinero Aparicio, et al.
Frontiers in Pediatrics
|
May 4, 2023
Case report: Gastroenterological management in a case of cardio-facio-cutaneous syndrome
B Ciacchini, G Di Nardo, M Marin, et al.
Journal of Medical Genetics
|
May 19, 2001
Suggestive linkage of situs inversus and other left-right axis anomalies to chromosome 6p
E Vitale, V Brancolini, A De Rienzo, et al.
American Journal of Human Genetics
|
August 1, 1997
A submicroscopic deletion in Xq26 associated with familial situs ambiguus
G B Ferrero, M Gebbia, G Pilia, et al.
Expert Opinion on Biological Therapy
|
March 13, 2009
Neutralizing antibodies in multiple sclerosis patients treated with 375 micrograms interferon-beta-1b
L Durelli, P Barbero, A Cucci, et al.
Autoimmunity Reviews
|
August 16, 2008
Anti-neuronal antibodies in patients with HCV-related mixed cryoglobulinemia
M Alpa, B Ferrero, R Cavallo, et al.
Page
of 10