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http://hdl.handle.net/11452/21370
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Sloan, Emily A. | - |
dc.contributor.author | Elizondo, Leah I. | - |
dc.contributor.author | Huang, Cheng | - |
dc.contributor.author | André, Jean-Luc | - |
dc.contributor.author | Bogdanovic, Radovan | - |
dc.contributor.author | Cockfield, Sandra | - |
dc.contributor.author | Cordeiro, Isabel | - |
dc.contributor.author | Deschenes, Georges | - |
dc.contributor.author | Fründ, Stefan | - |
dc.contributor.author | Kaitila, Ilkka | - |
dc.contributor.author | Lama, Giuliana | - |
dc.contributor.author | Lamfers, Petra | - |
dc.contributor.author | Lücke, Thomas | - |
dc.contributor.author | Milford, David V. | - |
dc.contributor.author | Najera, Lydia | - |
dc.contributor.author | Rodrigo, Francisco | - |
dc.contributor.author | Saraiva, Jorge M. | - |
dc.contributor.author | Schmidt, Beate | - |
dc.contributor.author | Smith, Graham C. | - |
dc.contributor.author | Stajic, Nastasa | - |
dc.contributor.author | Stein, Anja | - |
dc.contributor.author | Taha, Doris | - |
dc.contributor.author | Wand, Dorothea | - |
dc.contributor.author | Armstrong, Dawna | - |
dc.contributor.author | Boerkoel, Cornelius F. | - |
dc.date.accessioned | 2021-08-09T08:42:07Z | - |
dc.date.available | 2021-08-09T08:42:07Z | - |
dc.date.issued | 2005-07-01 | - |
dc.identifier.citation | Kılıç, S. Ş. vd. (2005). "Association of migraine-like headaches with schimke immuno-osseous dysplasia". American Journal of Medical Genetics Part A, 135A(2), 206-210. | en_US |
dc.identifier.issn | 1552-4825 | - |
dc.identifier.uri | https://doi.org/10.1002/ajmg.a.30692 | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.30692 | - |
dc.identifier.uri | http://hdl.handle.net/11452/21370 | - |
dc.description.abstract | Schimke immuno-osseous dysplasia (SIOD) is characterized by spondyloepiphyseal. dysplasia, nephropathy, and T-cell deficiency. SIOD is caused by mutations in the putative chromatin remodeling protein SAL&RCAL1. We report an 8-year-old boy with SIOD and recurrent, severe, refractory migraine-like headaches. Through a retrospective questionnaire-based study, we found that refractory and severely disabling migraine-like headaches occur in nearly half of SIOD patients. We have also found that the vasodilator minoxidil provided symptomatic relief for one patient. We hypothesize that these headaches may arise from an intrinsic vascular, neuroimmune, or neurovascular defect resulting from loss of SMARCAL1 function. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Migraine | en_US |
dc.subject | Immunodeficiency | en_US |
dc.subject | Skeletal dysplasia | en_US |
dc.subject | Headache | en_US |
dc.subject | Renal failure | en_US |
dc.subject | Nephrotic syndrome | en_US |
dc.subject | Immunoosseous dysplasia | en_US |
dc.subject | Spondyloepiphyseal dysplasia | en_US |
dc.subject | Disease | en_US |
dc.subject | Genetics & heredity | en_US |
dc.title | Association of migraine-like headaches with schimke immuno-osseous dysplasia | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000229488000019 | tr_TR |
dc.identifier.scopus | 2-s2.0-20044373274 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/İmmünoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Nefroloji Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0001-8571-2581 | tr_TR |
dc.identifier.startpage | 206 | tr_TR |
dc.identifier.endpage | 210 | tr_TR |
dc.identifier.volume | 135A | tr_TR |
dc.identifier.issue | 2 | tr_TR |
dc.relation.journal | American Journal of Medical Genetics Part A | tr_TR |
dc.contributor.buuauthor | Kılıç, Sara Şebnem | - |
dc.contributor.buuauthor | Dönmez, Osman | - |
dc.contributor.researcherid | AAH-1658-2021 | tr_TR |
dc.relation.collaboration | Yurt dışı | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.identifier.pubmed | 15884045 | tr_TR |
dc.subject.wos | Genetics & heredity | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | Pubmed | en_US |
dc.wos.quartile | Q3 | tr_TR |
dc.contributor.scopusid | 34975059200 | tr_TR |
dc.contributor.scopusid | 19033971800 | tr_TR |
dc.subject.emtree | Gene product | en_US |
dc.subject.emtree | Minoxidil | en_US |
dc.subject.emtree | Protein SMARCAL1 | en_US |
dc.subject.emtree | Unclassified drug | en_US |
dc.subject.emtree | Vasodilator agent | en_US |
dc.subject.emtree | Bone dysplasia | en_US |
dc.subject.emtree | Case report | en_US |
dc.subject.emtree | Child | en_US |
dc.subject.emtree | Disease association | en_US |
dc.subject.emtree | Gene mutation | en_US |
dc.subject.emtree | Headache | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Kidney disease | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Migraine | en_US |
dc.subject.emtree | Neuroimmunology | en_US |
dc.subject.emtree | Schimke immunoosseous dysplasia | en_US |
dc.subject.emtree | T cell depletion | en_US |
Appears in Collections: | Scopus Web of Science |
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