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Irina Giurgea

Showing results (1-10 of 81) with videos related to

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Behavior Research Methods|July 29, 2025
Reward as a facet of word meaning: Ratings of motivation for 8,601 English wordsDoina-Irina Giurgea, Penny M Pexman, Richard J Binney
Allergy|June 17, 2022
Absence of NLRP3 somatic mutations and VEXAS-related UBA1 mutations in a large cohort of patients with Schnitzler syndromeCamille Louvrier, Fawaz Awad, Serge Amselem, et al.
Seminars in Neonatology : SN|March 12, 2004
Neonatal hypoglycaemia: aetiologiesPascale de Lonlay, Irina Giurgea, Guy Touati, et al.
European Journal of Immunology|September 3, 2025
Baseline Single-Cell Differences in Polyfunctionality Between Systemic Autoinflammatory Diseases Patients and Healthy ControlsAline Linder, Farah Diab, Loïc de Pontual, et al.
Pediatric Neurology|January 25, 2005
Underdiagnosis of mild congenital disorders of glycosylation type IaIrina Giurgea, Anne Michel, Martine Le Merrer, et al.
L' Orthodontie Francaise|April 27, 2026
Differential diagnosis within primary molar retention: Characteristics of primary eruption failure versus primary retention of a single toothBeatriz Castañeda, Aline Lessa, Julie Galimand, et al.
Joint Bone Spine|February 3, 2020
Typical Familial Mediterranean Fever associated with the heterozygous missense sequence p.T577N variant of the MEFV gene: Report on two Northern European Caucasians relatives in FranceInes Elhani, Anael Dumont, Samuel Deshayes, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 24, 2005
Acute pancreatitis in paediatric systemic lupus erythematosusLaurence Perrin, Irina Giurgea, Valérie Baudet-Bonneville, et al.
Mechanisms of Ageing and Development|March 17, 2018
Photoaging and skin cancer: Is the inflammasome the missing link?Fawaz Awad, Eman Assrawi, Camille Louvrier, et al.
Indian Journal of Human Genetics|September 30, 2011
Mowat-Wilson syndrome in a Moroccan consanguineous familyIlham Ratbi, Chafai Siham Elalaoui, Moal Florence Dastot-Le, et al.
Pageof 9

Showing results (1-10 of 81) with videos related to

Sort By:
Pageof 9
Behavior Research Methods|July 29, 2025
Reward as a facet of word meaning: Ratings of motivation for 8,601 English wordsDoina-Irina Giurgea, Penny M Pexman, Richard J Binney
Allergy|June 17, 2022
Absence of NLRP3 somatic mutations and VEXAS-related UBA1 mutations in a large cohort of patients with Schnitzler syndromeCamille Louvrier, Fawaz Awad, Serge Amselem, et al.
Seminars in Neonatology : SN|March 12, 2004
Neonatal hypoglycaemia: aetiologiesPascale de Lonlay, Irina Giurgea, Guy Touati, et al.
European Journal of Immunology|September 3, 2025
Baseline Single-Cell Differences in Polyfunctionality Between Systemic Autoinflammatory Diseases Patients and Healthy ControlsAline Linder, Farah Diab, Loïc de Pontual, et al.
Pediatric Neurology|January 25, 2005
Underdiagnosis of mild congenital disorders of glycosylation type IaIrina Giurgea, Anne Michel, Martine Le Merrer, et al.
L' Orthodontie Francaise|April 27, 2026
Differential diagnosis within primary molar retention: Characteristics of primary eruption failure versus primary retention of a single toothBeatriz Castañeda, Aline Lessa, Julie Galimand, et al.
Joint Bone Spine|February 3, 2020
Typical Familial Mediterranean Fever associated with the heterozygous missense sequence p.T577N variant of the MEFV gene: Report on two Northern European Caucasians relatives in FranceInes Elhani, Anael Dumont, Samuel Deshayes, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 24, 2005
Acute pancreatitis in paediatric systemic lupus erythematosusLaurence Perrin, Irina Giurgea, Valérie Baudet-Bonneville, et al.
Mechanisms of Ageing and Development|March 17, 2018
Photoaging and skin cancer: Is the inflammasome the missing link?Fawaz Awad, Eman Assrawi, Camille Louvrier, et al.
Indian Journal of Human Genetics|September 30, 2011
Mowat-Wilson syndrome in a Moroccan consanguineous familyIlham Ratbi, Chafai Siham Elalaoui, Moal Florence Dastot-Le, et al.
Pageof 9