Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

I Giurgea

Showing results (1-10 of 20) with videos related to

Pageof 2
Sort By:
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 27, 2003
[Molecular tests and metabolic diseases]P de Lonlay, I Giurgea, J M Saudubray
Revista De Chirurgie, Oncologie, Radiologie, O.R.L., Oftalmologie, Stomatologie. Chirurgie|January 1, 1985
[Current problems in diagnosing and treating lymphedema of the limbs]A Kaufmann, F Galea, I Giurgea, et al.
Romanian Journal of Internal Medicine = Revue Roumaine De Medecine Interne|April 1, 1992
Heterozygous protein C deficiency and coumarin necrosis of the skinM Cucuianu, N Hagău, M Cotul, et al.
Clinical Dysmorphology|October 25, 2000
Congenital microgastria with Pierre Robin sequence and partial trismusI Giurgea, F Raqbi, C Nihoul-Fékété, et al.
Phlebologie|July 1, 1986
[Venous emergencies. Personal experience and viewpoint]A Kaufmann, A Andercou, I Giurgea, et al.
Revista De Chirurgie, Oncologie, Radiologie, O.R.L., Oftalmologie, Stomatologie. Chirurgie|January 1, 1988
[Gangrene of the extremities--terminology, classification and treatment. Our experience with 250 cases]A Kaufmann, A Andercou, F Galea, et al.
Journal of Medical Genetics|January 20, 2004
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndromeP Bénit, A Slama, F Cartault, et al.
La Revue De Medecine Interne|November 2, 2020
[Periodic fever syndrome associated with mutations in the TNF type 1 receptor gene: A differential diagnosis of familial Mediterranean fever that should not be overlooked in patients of Mediterranean origin]R Bourguiba, L Savey, A Aouba, et al.
Molecular Genetics and Metabolism|November 3, 2005
Deoxyguanosine kinase mutations and combined deficiencies of the mitochondrial respiratory chain in patients with hepatic involvementA Slama, I Giurgea, D Debrey, et al.
Journal of Medical Genetics|December 20, 2003
Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiencyS Lebon, M Chol, P Benit, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 27, 2003
[Molecular tests and metabolic diseases]P de Lonlay, I Giurgea, J M Saudubray
Revista De Chirurgie, Oncologie, Radiologie, O.R.L., Oftalmologie, Stomatologie. Chirurgie|January 1, 1985
[Current problems in diagnosing and treating lymphedema of the limbs]A Kaufmann, F Galea, I Giurgea, et al.
Romanian Journal of Internal Medicine = Revue Roumaine De Medecine Interne|April 1, 1992
Heterozygous protein C deficiency and coumarin necrosis of the skinM Cucuianu, N Hagău, M Cotul, et al.
Clinical Dysmorphology|October 25, 2000
Congenital microgastria with Pierre Robin sequence and partial trismusI Giurgea, F Raqbi, C Nihoul-Fékété, et al.
Phlebologie|July 1, 1986
[Venous emergencies. Personal experience and viewpoint]A Kaufmann, A Andercou, I Giurgea, et al.
Revista De Chirurgie, Oncologie, Radiologie, O.R.L., Oftalmologie, Stomatologie. Chirurgie|January 1, 1988
[Gangrene of the extremities--terminology, classification and treatment. Our experience with 250 cases]A Kaufmann, A Andercou, F Galea, et al.
Journal of Medical Genetics|January 20, 2004
Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndromeP Bénit, A Slama, F Cartault, et al.
La Revue De Medecine Interne|November 2, 2020
[Periodic fever syndrome associated with mutations in the TNF type 1 receptor gene: A differential diagnosis of familial Mediterranean fever that should not be overlooked in patients of Mediterranean origin]R Bourguiba, L Savey, A Aouba, et al.
Molecular Genetics and Metabolism|November 3, 2005
Deoxyguanosine kinase mutations and combined deficiencies of the mitochondrial respiratory chain in patients with hepatic involvementA Slama, I Giurgea, D Debrey, et al.
Journal of Medical Genetics|December 20, 2003
Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiencyS Lebon, M Chol, P Benit, et al.
Pageof 2