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Pescia

Showing results (191-200 of 242) with videos related to

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Human Genetics|July 1, 1992
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility geneF Munier, M A Spence, G Pescia, et al.
The Annals of Thoracic Surgery|October 26, 2005
Respiratory dependent compression of a venous bypass: therapy by stentingMarkus J Wilhelm, Martin Igual, Raymond Mury, et al.
American Journal of Human Genetics|December 5, 1998
Evidence of somatic and germinal mosaicism in pseudo-low-penetrant hereditary retinoblastoma, by constitutional and single-sperm mutation analysisF L Munier, F Thonney, A Girardet, et al.
Chirurgia Italiana|October 1, 1980
[Indications for cerebral revascularization surgery (author's transl)]F Bianchetti, I Cioffi, F Castiglioni, et al.
Physical Review Letters|August 25, 2004
Fourier transform imaging of spin vortex eigenmodesM Buess, R Höllinger, T Haug, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOXE Korvatska, F L Munier, L Zografos, et al.
Proceedings. Mathematical, Physical, and Engineering Sciences|December 14, 2016
Thirty per cent contrast in secondary-electron imaging by scanning field-emission microscopyD A Zanin, L G De Pietro, Q Peter, et al.
Journal of Clinical Medicine|November 13, 2021
Lymphocytic Infiltrate and p53 Protein Expression as Predictive Markers of Response and Outcome in Myelodysplastic Syndromes Treated with AzacitidineCarlo Pescia, Francesca Boggio, Giorgio Alberto Croci, et al.
Schweizerische Medizinische Wochenschrift|December 13, 1975
[The diagnosis of liver metastases and primary hepatomas by means of scintigraphy, laparoscopy and laparotomy]C A Horica, R Pescia, A Akovbiantz, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigreesF L Munier, M X Wang, M A Spence, et al.
Pageof 25

Showing results (191-200 of 242) with videos related to

Sort By:
Pageof 25
Human Genetics|July 1, 1992
Paternal selection favoring mutant alleles of the retinoblastoma susceptibility geneF Munier, M A Spence, G Pescia, et al.
The Annals of Thoracic Surgery|October 26, 2005
Respiratory dependent compression of a venous bypass: therapy by stentingMarkus J Wilhelm, Martin Igual, Raymond Mury, et al.
American Journal of Human Genetics|December 5, 1998
Evidence of somatic and germinal mosaicism in pseudo-low-penetrant hereditary retinoblastoma, by constitutional and single-sperm mutation analysisF L Munier, F Thonney, A Girardet, et al.
Chirurgia Italiana|October 1, 1980
[Indications for cerebral revascularization surgery (author's transl)]F Bianchetti, I Cioffi, F Castiglioni, et al.
Physical Review Letters|August 25, 2004
Fourier transform imaging of spin vortex eigenmodesM Buess, R Höllinger, T Haug, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOXE Korvatska, F L Munier, L Zografos, et al.
Proceedings. Mathematical, Physical, and Engineering Sciences|December 14, 2016
Thirty per cent contrast in secondary-electron imaging by scanning field-emission microscopyD A Zanin, L G De Pietro, Q Peter, et al.
Journal of Clinical Medicine|November 13, 2021
Lymphocytic Infiltrate and p53 Protein Expression as Predictive Markers of Response and Outcome in Myelodysplastic Syndromes Treated with AzacitidineCarlo Pescia, Francesca Boggio, Giorgio Alberto Croci, et al.
Schweizerische Medizinische Wochenschrift|December 13, 1975
[The diagnosis of liver metastases and primary hepatomas by means of scintigraphy, laparoscopy and laparotomy]C A Horica, R Pescia, A Akovbiantz, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigreesF L Munier, M X Wang, M A Spence, et al.
Pageof 25