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American Journal of Medical Genetics
|
January 31, 1998
Retinitis pigmentosa, hypopituitarism, nephronophthisis, and mild skeletal dysplasia (RHYNS): a new syndrome?
M Di Rocco, P Picco, A Arslanian, et al.
Journal of the Neurological Sciences
|
July 1, 1992
Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibers
G L Mancardi, M Di Rocco, A Schenone, et al.
Tissue Antigens
|
January 6, 2001
Sequence analysis of a new HLA-DR11 allele in a Caucasian Italian family: DRB1*11272
A Canossi, D Piancatelli, F Papola, et al.
European Journal of Pediatrics
|
August 1, 1993
Diagnostic difficulties and positive therapeutic response in a patient with sinus histiocytosis with massive lymphadenopathy
P Picco, A Buoncompagni, V Pistoia, et al.
Journal of Inherited Metabolic Disease
|
July 10, 1999
3-Methylglutaconic aciduria and hypermethioninaemia in a child with clinical and neuroradiological findings of Leigh disease
M Di Rocco, U Caruso, I Moroni, et al.
Neurology
|
December 25, 2003
Leukoencephalopathy with vanishing white matter:: an adult onset case
R Biancheri, A Rossi, M Di Rocco, et al.
Cancer Biotherapy & Radiopharmaceuticals
|
December 1, 1996
Necessity of biotherapeutic treatments inducing TH1 cell functions in colorectal cancer
I Contasta, P Pellegrini, A M Berghella, et al.
Journal of Applied Microbiology
|
October 10, 2013
The effectiveness of domestic cook on inactivation of murine norovirus in experimentally infected Manila clams (Ruditapes philippinarum)
A Toffan, A Brutti, A De Pasquale, et al.
Transplantation Proceedings
|
December 1, 1993
Genotyping analysis of HLA class II genes in donor-recipient kidney transplant pairs
F Papola, A Canossi, M Valeri, et al.
Human Mutation
|
June 29, 2004
Screening of 25 Italian patients with Niemann-Pick A reveals fourteen new mutations, one common and thirteen private, in SMPD1
V Ricci, M Stroppiano, F Corsolini, et al.
Page
of 12
Search research articles
Search
Showing results (71-80 of 115) with videos related to
Sort By:
Page
of 12
American Journal of Medical Genetics
|
January 31, 1998
Retinitis pigmentosa, hypopituitarism, nephronophthisis, and mild skeletal dysplasia (RHYNS): a new syndrome?
M Di Rocco, P Picco, A Arslanian, et al.
Journal of the Neurological Sciences
|
July 1, 1992
Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibers
G L Mancardi, M Di Rocco, A Schenone, et al.
Tissue Antigens
|
January 6, 2001
Sequence analysis of a new HLA-DR11 allele in a Caucasian Italian family: DRB1*11272
A Canossi, D Piancatelli, F Papola, et al.
European Journal of Pediatrics
|
August 1, 1993
Diagnostic difficulties and positive therapeutic response in a patient with sinus histiocytosis with massive lymphadenopathy
P Picco, A Buoncompagni, V Pistoia, et al.
Journal of Inherited Metabolic Disease
|
July 10, 1999
3-Methylglutaconic aciduria and hypermethioninaemia in a child with clinical and neuroradiological findings of Leigh disease
M Di Rocco, U Caruso, I Moroni, et al.
Neurology
|
December 25, 2003
Leukoencephalopathy with vanishing white matter:: an adult onset case
R Biancheri, A Rossi, M Di Rocco, et al.
Cancer Biotherapy & Radiopharmaceuticals
|
December 1, 1996
Necessity of biotherapeutic treatments inducing TH1 cell functions in colorectal cancer
I Contasta, P Pellegrini, A M Berghella, et al.
Journal of Applied Microbiology
|
October 10, 2013
The effectiveness of domestic cook on inactivation of murine norovirus in experimentally infected Manila clams (Ruditapes philippinarum)
A Toffan, A Brutti, A De Pasquale, et al.
Transplantation Proceedings
|
December 1, 1993
Genotyping analysis of HLA class II genes in donor-recipient kidney transplant pairs
F Papola, A Canossi, M Valeri, et al.
Human Mutation
|
June 29, 2004
Screening of 25 Italian patients with Niemann-Pick A reveals fourteen new mutations, one common and thirteen private, in SMPD1
V Ricci, M Stroppiano, F Corsolini, et al.
Page
of 12