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Showing results (121-130 of 228) with videos related to

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Pathologie-Biologie|September 1, 1978
beta2-Microglobulin in lymphoproliferative disorders with special reference to gammapathiesJ P Cassuto, B P Krebs, M V Joyner, et al.
Prenatal Diagnosis|January 21, 2003
Congenital erythropoietic porphyria (Günther's disease): two cases with very early prenatal manifestation and cystic hygromaE Pannier, G Viot, M C Aubry, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 15, 2002
Prenatal diagnosis of fetal tail and postabortum anatomical descriptionG Grangé, J Tantau, E Pannier, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|June 9, 2015
Two-year post-transplantation cytomegalovirus DNAemia in asymptomatic kidney transplant recipients: incidence, risk factors, and outcomeB Viot, I Garrigue, B Taton, et al.
American Journal of Clinical Pathology|July 13, 2014
Neonatal Silver-Russell syndrome with maternal uniparental heterodisomy, trisomy 7 mosaicism, and dysplasia of the cerebellumFatma Abdelhedi, Laila El Khattabi, Laurence Cuisset, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|September 7, 2000
Systematic percutaneous fluoroscopic gastrostomy for concomitant radiochemotherapy of advanced head and neck cancer: optimization of therapyP Y Marcy, N Magné, R J Bensadoun, et al.
American Journal of Medical Genetics|April 15, 2000
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicismL Faivre, G Viot, M Prieur, et al.
Gastroenterologie Clinique Et Biologique|April 1, 1989
[Biopsies of the endoscopically normal rectum and colon: a necessity. Incidence of collagen colitis and microscopic colitis]J L Gineston, H Sevestre, P Descombes, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Chediak-Higashi syndrome associated with maternal uniparental isodisomy of chromosome 1R Dufourcq-Lagelouse, N Lambert, M Duval, et al.
European Journal of Pediatrics|December 3, 1998
Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomaliesL Iserin, P de Lonlay, G Viot, et al.
Pageof 23

Showing results (121-130 of 228) with videos related to

Sort By:
Pageof 23
Pathologie-Biologie|September 1, 1978
beta2-Microglobulin in lymphoproliferative disorders with special reference to gammapathiesJ P Cassuto, B P Krebs, M V Joyner, et al.
Prenatal Diagnosis|January 21, 2003
Congenital erythropoietic porphyria (Günther's disease): two cases with very early prenatal manifestation and cystic hygromaE Pannier, G Viot, M C Aubry, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 15, 2002
Prenatal diagnosis of fetal tail and postabortum anatomical descriptionG Grangé, J Tantau, E Pannier, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|June 9, 2015
Two-year post-transplantation cytomegalovirus DNAemia in asymptomatic kidney transplant recipients: incidence, risk factors, and outcomeB Viot, I Garrigue, B Taton, et al.
American Journal of Clinical Pathology|July 13, 2014
Neonatal Silver-Russell syndrome with maternal uniparental heterodisomy, trisomy 7 mosaicism, and dysplasia of the cerebellumFatma Abdelhedi, Laila El Khattabi, Laurence Cuisset, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|September 7, 2000
Systematic percutaneous fluoroscopic gastrostomy for concomitant radiochemotherapy of advanced head and neck cancer: optimization of therapyP Y Marcy, N Magné, R J Bensadoun, et al.
American Journal of Medical Genetics|April 15, 2000
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicismL Faivre, G Viot, M Prieur, et al.
Gastroenterologie Clinique Et Biologique|April 1, 1989
[Biopsies of the endoscopically normal rectum and colon: a necessity. Incidence of collagen colitis and microscopic colitis]J L Gineston, H Sevestre, P Descombes, et al.
European Journal of Human Genetics : EJHG|September 14, 1999
Chediak-Higashi syndrome associated with maternal uniparental isodisomy of chromosome 1R Dufourcq-Lagelouse, N Lambert, M Duval, et al.
European Journal of Pediatrics|December 3, 1998
Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomaliesL Iserin, P de Lonlay, G Viot, et al.
Pageof 23