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A Pizzuti

Showing results (111-120 of 117) with videos related to

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European Heart Journal|March 27, 2002
Clinical value of left atrial appendage flow velocity for predicting of cardioversion success in patients with non-valvular atrial fibrillationA Pálinkás, E Antonielli, E Picano, et al.
American Journal of Human Genetics|June 12, 1999
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11R Wadey, J McKie, C Papapetrou, et al.
Biochimica Et Biophysica Acta|April 16, 1998
Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L)G Novelli, A Mari, F Amati, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 5, 2008
Case report of adult-onset Allgrove syndromeF Gilio, S Di Rezze, A Conte, et al.
American Journal of Human Genetics|April 1, 1996
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndromeA Pizzuti, G Novelli, A Mari, et al.
Diabetes|June 27, 2000
A PC-1 amino acid variant (K121Q) is associated with faster progression of renal disease in patients with type 1 diabetes and albuminuriaS De Cosmo, A Argiolas, G Miscio, et al.
Skin Health and Disease|June 6, 2022
Single-nucleotide polymorphisms in 3'-untranslated region inducible costimulator gene and the important roles of miRNA in alopecia areataG Conteduca, A Rossi, F Megiorni, et al.
Pageof 12

Showing results (111-120 of 117) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 117 results.
European Heart Journal|March 27, 2002
Clinical value of left atrial appendage flow velocity for predicting of cardioversion success in patients with non-valvular atrial fibrillationA Pálinkás, E Antonielli, E Picano, et al.
American Journal of Human Genetics|June 12, 1999
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11R Wadey, J McKie, C Papapetrou, et al.
Biochimica Et Biophysica Acta|April 16, 1998
Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L)G Novelli, A Mari, F Amati, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 5, 2008
Case report of adult-onset Allgrove syndromeF Gilio, S Di Rezze, A Conte, et al.
American Journal of Human Genetics|April 1, 1996
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndromeA Pizzuti, G Novelli, A Mari, et al.
Diabetes|June 27, 2000
A PC-1 amino acid variant (K121Q) is associated with faster progression of renal disease in patients with type 1 diabetes and albuminuriaS De Cosmo, A Argiolas, G Miscio, et al.
Skin Health and Disease|June 6, 2022
Single-nucleotide polymorphisms in 3'-untranslated region inducible costimulator gene and the important roles of miRNA in alopecia areataG Conteduca, A Rossi, F Megiorni, et al.
Pageof 12