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A Martini

Showing results (571-580 of 635) with videos related to

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American Journal of Medical Genetics|September 20, 2002
Exploring the clinical and epidemiological complexity of GJB2-linked deafnessF Gualandi, A Ravani, A Berto, et al.
European Review for Medical and Pharmacological Sciences|December 18, 2012
Ruthenium-106 eye plaque brachytherapy in the conservative treatment of uveal melanoma: a mono-institutional experienceP Perri, F Fiorica, S D'Angelo, et al.
Vaccine|June 21, 2024
Vaccine effectiveness of 3rd generation mpox vaccines against mpox and disease severity: A systematic review and meta-analysisLauren Pischel, Brett A Martini, Natalle Yu, et al.
Resuscitation|October 4, 2015
Anxiety and depression among out-of-hospital cardiac arrest survivorsG Lilja, G Nilsson, N Nielsen, et al.
Clinical and Experimental Rheumatology|August 21, 2001
The Serbian version of the Childhood Health Assessment Questionnaire (CHAQ) and the Child Health Questionnaire (CHQ)G Susic, N Ruperto, R Stojanovic, et al.
Annals of the Rheumatic Diseases|July 6, 2012
MRI versus conventional measures of disease activity and structural damage in evaluating treatment efficacy in juvenile idiopathic arthritisC Malattia, A Consolaro, S Pederzoli, et al.
Pediatric Rheumatology Online Journal|July 10, 2019
Whole exome sequencing approach to childhood onset familial erythrodermic psoriasis unravels a novel mutation of CARD14 requiring unusual high doses of ustekinumabS Signa, E Campione, M Rusmini, et al.
Journal of Affective Disorders|July 7, 2024
Synthesising 30 years of clinical experience and scientific insight on affective temperaments in psychiatric disorders: State of the artE Favaretto, F Bedani, G E Brancati, et al.
Clinical and Experimental Rheumatology|April 16, 1998
Oral versus intramuscular methotrexate in juvenile chronic arthritis. Italian Pediatric Rheumatology Study GroupA Ravelli, V Gerloni, F Corona, et al.
American Journal of Human Genetics|March 23, 2000
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIaM D Weston, J D Eudy, S Fujita, et al.
Pageof 64

Showing results (571-580 of 635) with videos related to

Sort By:
Pageof 64
American Journal of Medical Genetics|September 20, 2002
Exploring the clinical and epidemiological complexity of GJB2-linked deafnessF Gualandi, A Ravani, A Berto, et al.
European Review for Medical and Pharmacological Sciences|December 18, 2012
Ruthenium-106 eye plaque brachytherapy in the conservative treatment of uveal melanoma: a mono-institutional experienceP Perri, F Fiorica, S D'Angelo, et al.
Vaccine|June 21, 2024
Vaccine effectiveness of 3rd generation mpox vaccines against mpox and disease severity: A systematic review and meta-analysisLauren Pischel, Brett A Martini, Natalle Yu, et al.
Resuscitation|October 4, 2015
Anxiety and depression among out-of-hospital cardiac arrest survivorsG Lilja, G Nilsson, N Nielsen, et al.
Clinical and Experimental Rheumatology|August 21, 2001
The Serbian version of the Childhood Health Assessment Questionnaire (CHAQ) and the Child Health Questionnaire (CHQ)G Susic, N Ruperto, R Stojanovic, et al.
Annals of the Rheumatic Diseases|July 6, 2012
MRI versus conventional measures of disease activity and structural damage in evaluating treatment efficacy in juvenile idiopathic arthritisC Malattia, A Consolaro, S Pederzoli, et al.
Pediatric Rheumatology Online Journal|July 10, 2019
Whole exome sequencing approach to childhood onset familial erythrodermic psoriasis unravels a novel mutation of CARD14 requiring unusual high doses of ustekinumabS Signa, E Campione, M Rusmini, et al.
Journal of Affective Disorders|July 7, 2024
Synthesising 30 years of clinical experience and scientific insight on affective temperaments in psychiatric disorders: State of the artE Favaretto, F Bedani, G E Brancati, et al.
Clinical and Experimental Rheumatology|April 16, 1998
Oral versus intramuscular methotrexate in juvenile chronic arthritis. Italian Pediatric Rheumatology Study GroupA Ravelli, V Gerloni, F Corona, et al.
American Journal of Human Genetics|March 23, 2000
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIaM D Weston, J D Eudy, S Fujita, et al.
Pageof 64