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Neuropediatrics
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March 30, 2011
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis
P Pavone, M Pettoello-Mantovano, A Le Pira, et al.
Neuropediatrics
|
January 4, 2005
Fetal cells in maternal blood: a six-fold increase in women who have undergone amniocentesis and carry a fetus with Down syndrome: a multicenter study
E Falcidia, E Parano, A Grillo, et al.
International Journal of Immunopathology and Pharmacology
|
October 4, 2014
Pediatric autoimmune neuropsychiatric disorder associated with group a streptococcal infection: the role of surgical treatment
P Pavone, V Rapisarda, A Serra, et al.
Nature Genetics
|
February 14, 1998
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa
P Banerjee, P W Kleyn, J A Knowles, et al.
Human Molecular Genetics
|
February 1, 1997
A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions
T A Carter, C G Bönnemann, C H Wang, et al.
American Journal of Human Genetics
|
August 1, 1997
Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses
A B Shah, I Chernov, H T Zhang, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 66) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 66 results.
Neuropediatrics
|
March 30, 2011
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis
P Pavone, M Pettoello-Mantovano, A Le Pira, et al.
Neuropediatrics
|
January 4, 2005
Fetal cells in maternal blood: a six-fold increase in women who have undergone amniocentesis and carry a fetus with Down syndrome: a multicenter study
E Falcidia, E Parano, A Grillo, et al.
International Journal of Immunopathology and Pharmacology
|
October 4, 2014
Pediatric autoimmune neuropsychiatric disorder associated with group a streptococcal infection: the role of surgical treatment
P Pavone, V Rapisarda, A Serra, et al.
Nature Genetics
|
February 14, 1998
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa
P Banerjee, P W Kleyn, J A Knowles, et al.
Human Molecular Genetics
|
February 1, 1997
A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions
T A Carter, C G Bönnemann, C H Wang, et al.
American Journal of Human Genetics
|
August 1, 1997
Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses
A B Shah, I Chernov, H T Zhang, et al.
Page
of 7