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C Douillard

Showing results (11-20 of 16) with videos related to

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La Revue De Medecine Interne|November 16, 2016
[Acute arterial thrombosis in a context of hyperhomocysteinemia: Case report and literature review]G Raybaud, M Lambert, C Douillard, et al.
Annales D'Endocrinologie|January 16, 2003
Vitamin D deficiency and severe hyperparathyroidismS Jonard, M Gauthier-Morgenstern, C Douillard, et al.
Thyroid : Official Journal of the American Thyroid Association|December 14, 2004
Thyroid carcinomas involving follicular and parafollicular C cells: seventeen cases with characterization of RET oncogenic activationM-C Vantyghem, P Pigny, E Leteurtre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 20, 2018
Transition from pediatric to adult care in adolescents with hereditary metabolic diseases: Specific guidelines from the French network for rare inherited metabolic diseases (G2M)B Chabrol, P Jacquin, L Francois, et al.
La Revue De Medecine Interne|November 26, 2016
[Acid sphingomyelinase deficiency (Niemann-Pick disease type B) in adulthood: A retrospective multicentric study of 28 adult cases]O Lidove, N Belmatoug, R Froissart, et al.
Journal of Inherited Metabolic Disease|March 13, 2026
Long-Term Follow-Up of Patients With Transaldolase DeficiencyM Scaglione, A Brassier, A Wiedemann, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
La Revue De Medecine Interne|November 16, 2016
[Acute arterial thrombosis in a context of hyperhomocysteinemia: Case report and literature review]G Raybaud, M Lambert, C Douillard, et al.
Annales D'Endocrinologie|January 16, 2003
Vitamin D deficiency and severe hyperparathyroidismS Jonard, M Gauthier-Morgenstern, C Douillard, et al.
Thyroid : Official Journal of the American Thyroid Association|December 14, 2004
Thyroid carcinomas involving follicular and parafollicular C cells: seventeen cases with characterization of RET oncogenic activationM-C Vantyghem, P Pigny, E Leteurtre, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 20, 2018
Transition from pediatric to adult care in adolescents with hereditary metabolic diseases: Specific guidelines from the French network for rare inherited metabolic diseases (G2M)B Chabrol, P Jacquin, L Francois, et al.
La Revue De Medecine Interne|November 26, 2016
[Acid sphingomyelinase deficiency (Niemann-Pick disease type B) in adulthood: A retrospective multicentric study of 28 adult cases]O Lidove, N Belmatoug, R Froissart, et al.
Journal of Inherited Metabolic Disease|March 13, 2026
Long-Term Follow-Up of Patients With Transaldolase DeficiencyM Scaglione, A Brassier, A Wiedemann, et al.
Pageof 2