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Catheline Vilain

Showing results (1-10 of 58) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|February 19, 2004
Small amplified RNA-SAGECatheline Vilain, Gilbert Vassart
Case Reports in Pediatrics|August 4, 2017
First Report on Fetal Cerebral Polyglucosan Bodies in Mucopolysaccharidosis Type VIIHazim Kadhim, Valérie Segers, Catheline Vilain, et al.
Nucleic Acids Research|March 11, 2003
Small amplified RNA-SAGE: an alternative approach to study transcriptome from limiting amount of mRNACatheline Vilain, Frederick Libert, David Venet, et al.
Journal of the American Society of Nephrology : JASN|January 19, 2007
Nephrogenic syndrome of inappropriate antidiuresis in adults: high phenotypic variability in men and women from a large pedigreeGuy Decaux, Frédéric Vandergheynst, Yasmina Bouko, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 20, 2020
Homozygous p.R31H GNRH1 mutation and normosmic congenital hypogonadotropic hypogonadism in a patient and self-limited delayed puberty in his relativesCécile Brachet, Caroline Gernay, Emese Boros, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 26, 2011
"Benign" myoclonic epilepsy of infancy as the initial presentation of glucose transporter-1 deficiencyNicolas Gaspard, Arvid Suls, Catheline Vilain, et al.
Skin Appendage Disorders|January 12, 2023
Co-Occurrence of Hypohidrotic Ectodermal Dysplasia and Food Protein-Induced Enterocolitis Syndrome: A Report of a New Ectodysplasin A VariantDéborah Salik, Florine Moulart, Martina Marangoni, et al.
European Journal of Endocrinology|August 6, 2024
Hypothyroidism due to biallelic variants in IYD: description of 4 families and a novel variantEmese Boros, Catheline Vilain, Natacha Driessens, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 20, 2016
RFT1-congenital disorder of glycosylation (CDG) syndrome: a cause of early-onset severe epilepsyAlec Aeby, Cynthia Prigogine, Catheline Vilain, et al.
Journal of Medical Case Reports|June 22, 2025
Severe rhabdomyolysis in an infant due to fatty acid oxidation disorder: a case reportAmelie Krug, Pascale Perlot, Aurelie Empain, et al.
Pageof 6

Showing results (1-10 of 58) with videos related to

Sort By:
Pageof 6
Methods in Molecular Biology (Clifton, N.J.)|February 19, 2004
Small amplified RNA-SAGECatheline Vilain, Gilbert Vassart
Case Reports in Pediatrics|August 4, 2017
First Report on Fetal Cerebral Polyglucosan Bodies in Mucopolysaccharidosis Type VIIHazim Kadhim, Valérie Segers, Catheline Vilain, et al.
Nucleic Acids Research|March 11, 2003
Small amplified RNA-SAGE: an alternative approach to study transcriptome from limiting amount of mRNACatheline Vilain, Frederick Libert, David Venet, et al.
Journal of the American Society of Nephrology : JASN|January 19, 2007
Nephrogenic syndrome of inappropriate antidiuresis in adults: high phenotypic variability in men and women from a large pedigreeGuy Decaux, Frédéric Vandergheynst, Yasmina Bouko, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 20, 2020
Homozygous p.R31H GNRH1 mutation and normosmic congenital hypogonadotropic hypogonadism in a patient and self-limited delayed puberty in his relativesCécile Brachet, Caroline Gernay, Emese Boros, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 26, 2011
"Benign" myoclonic epilepsy of infancy as the initial presentation of glucose transporter-1 deficiencyNicolas Gaspard, Arvid Suls, Catheline Vilain, et al.
Skin Appendage Disorders|January 12, 2023
Co-Occurrence of Hypohidrotic Ectodermal Dysplasia and Food Protein-Induced Enterocolitis Syndrome: A Report of a New Ectodysplasin A VariantDéborah Salik, Florine Moulart, Martina Marangoni, et al.
European Journal of Endocrinology|August 6, 2024
Hypothyroidism due to biallelic variants in IYD: description of 4 families and a novel variantEmese Boros, Catheline Vilain, Natacha Driessens, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 20, 2016
RFT1-congenital disorder of glycosylation (CDG) syndrome: a cause of early-onset severe epilepsyAlec Aeby, Cynthia Prigogine, Catheline Vilain, et al.
Journal of Medical Case Reports|June 22, 2025
Severe rhabdomyolysis in an infant due to fatty acid oxidation disorder: a case reportAmelie Krug, Pascale Perlot, Aurelie Empain, et al.
Pageof 6