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Showing results (191-200 of 200) with videos related to

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Genes and Immunity|April 9, 2004
Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosisE Aganna, P N Hawkins, S Ozen, et al.
Nephron. Clinical Practice|May 15, 2009
Henoch-Schönlein nephritis: a nationwide studyO Soylemezoglu, O Ozkaya, S Ozen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 1998
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosisF E Karet, F J Gainza, A Z Györy, et al.
Annals of the Rheumatic Diseases|July 20, 2014
Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever RegistryR Levy, L Gérard, J Kuemmerle-Deschner, et al.
Annals of the Rheumatic Diseases|June 5, 2012
Guidelines for the genetic diagnosis of hereditary recurrent feversY Shinar, L Obici, I Aksentijevich, et al.
Annals of the Rheumatic Diseases|August 23, 2013
The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registryH J Lachmann, R Papa, K Gerhold, et al.
Clinical Immunology (Orlando, Fla.)|March 19, 2023
PReS-endorsed international childhood lupus T2T task force definition of childhood lupus low disease activity state (cLLDAS)E M D Smith, A Aggarwal, J Ainsworth, et al.
Nature Genetics|January 23, 1999
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafnessF E Karet, K E Finberg, R D Nelson, et al.
Arthritis and Rheumatism|October 10, 2012
2012 revised International Chapel Hill Consensus Conference Nomenclature of VasculitidesJ C Jennette, R J Falk, P A Bacon, et al.
Journal of Medical Genetics|November 5, 2002
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing lossE H Stover, K J Borthwick, C Bavalia, et al.
Pageof 20

Showing results (191-200 of 200) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 200 results.
Genes and Immunity|April 9, 2004
Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosisE Aganna, P N Hawkins, S Ozen, et al.
Nephron. Clinical Practice|May 15, 2009
Henoch-Schönlein nephritis: a nationwide studyO Soylemezoglu, O Ozkaya, S Ozen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 1998
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosisF E Karet, F J Gainza, A Z Györy, et al.
Annals of the Rheumatic Diseases|July 20, 2014
Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever RegistryR Levy, L Gérard, J Kuemmerle-Deschner, et al.
Annals of the Rheumatic Diseases|June 5, 2012
Guidelines for the genetic diagnosis of hereditary recurrent feversY Shinar, L Obici, I Aksentijevich, et al.
Annals of the Rheumatic Diseases|August 23, 2013
The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registryH J Lachmann, R Papa, K Gerhold, et al.
Clinical Immunology (Orlando, Fla.)|March 19, 2023
PReS-endorsed international childhood lupus T2T task force definition of childhood lupus low disease activity state (cLLDAS)E M D Smith, A Aggarwal, J Ainsworth, et al.
Nature Genetics|January 23, 1999
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafnessF E Karet, K E Finberg, R D Nelson, et al.
Arthritis and Rheumatism|October 10, 2012
2012 revised International Chapel Hill Consensus Conference Nomenclature of VasculitidesJ C Jennette, R J Falk, P A Bacon, et al.
Journal of Medical Genetics|November 5, 2002
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing lossE H Stover, K J Borthwick, C Bavalia, et al.
Pageof 20