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E Parano

Showing results (61-70 of 66) with videos related to

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Neuropediatrics|March 30, 2011
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysisP 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 studyE 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 treatmentP Pavone, V Rapisarda, A Serra, et al.
Nature Genetics|February 14, 1998
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosaP 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 deletionsT 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 analysesA B Shah, I Chernov, H T Zhang, et al.
Pageof 7

Showing results (61-70 of 66) with videos related to

Sort By:
Pageof 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-analysisP 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 studyE 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 treatmentP Pavone, V Rapisarda, A Serra, et al.
Nature Genetics|February 14, 1998
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosaP 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 deletionsT 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 analysesA B Shah, I Chernov, H T Zhang, et al.
Pageof 7