194 related articles for article (PubMed ID: 33098164)
1. Identification of Cytochrome b-245, beta-chain gene mutations, and clinical presentations in Iranian patients with X-linked chronic granulomatous disease.
Heydari A; Abolnezhadian F; Sadeghi-Shabestari M; Saberi A; Shamsizadeh A; Ghadiri AA; Ghandil P
J Clin Lab Anal; 2021 Feb; 35(2):e23637. PubMed ID: 33098164
[TBL] [Abstract][Full Text] [Related]
2. Novel mutations in CYBB Gene Cause X-linked chronic Granulomatous Disease in Pakistani patients.
Gul I; Khan TA; Akbar NU; Gul N; Ali R; Khan SN
Ital J Pediatr; 2023 Aug; 49(1):95. PubMed ID: 37533075
[TBL] [Abstract][Full Text] [Related]
3. Characterization of 4 New Mutations in the CYBB Gene in 10 Iranian Families With X-linked Chronic Granulomatous Disease.
Teimourian S; Sazgara F; de Boer M; van Leeuwen K; Roos D; Lashkary S; Chavoshzadeh Z; Nabavi M; Bemanian MH; Isaian A
J Pediatr Hematol Oncol; 2018 Jul; 40(5):e268-e272. PubMed ID: 29702544
[TBL] [Abstract][Full Text] [Related]
4. Three novel mutations in CYBA among 22 Iranians with Chronic granulomatous disease.
Badalzadeh M; Tajik S; Fazlollahi MR; Houshmand M; Fattahi F; Alizadeh Z; Movahedi M; Adab Z; Khotaei GT; Hamidieh AA; Heidarnazhad H; Pourpak Z
Int J Immunogenet; 2017 Dec; 44(6):314-321. PubMed ID: 28941186
[TBL] [Abstract][Full Text] [Related]
5. Exon skipping in CYBB mRNA and skewed inactivation of X chromosome cause late-onset chronic granulomatous disease.
Eguchi M; Yagi C; Tauchi H; Kobayashi M; Ishii E; Eguchi-Ishimae M
Pediatr Hematol Oncol; 2018; 35(5-6):341-349. PubMed ID: 30633606
[TBL] [Abstract][Full Text] [Related]
6. De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE-1 Element Insertion Resulting in Chronic Granulomatous Disease.
Yu L; Li W; Lv G; Sun G; Yang L; Chen J; Zhou L; Ding Y; Zhang Z; Tang X; An Y; Zhao X
J Clin Immunol; 2023 Jan; 43(1):88-100. PubMed ID: 35997928
[TBL] [Abstract][Full Text] [Related]
7. Hematologically important mutations: X-linked chronic granulomatous disease (fourth update).
Roos D; van Leeuwen K; Hsu AP; Priel DL; Begtrup A; Brandon R; Stasia MJ; Bakri FG; Köker N; Köker MY; Madkaika M; de Boer M; Garcia-Morato MB; Shephard JLV; Roesler J; Kanegane H; Kawai T; Di Matteo G; Shahrooei M; Bustamante J; Rawat A; Vignesh P; Mortaz E; Fayezi A; Cagdas D; Tezcan I; Kitcharoensakkul M; Dinauer MC; Meyts I; Wolach B; Condino-Neto A; Zerbe CS; Holland SM; Malech HL; Gallin JI; Kuhns DB
Blood Cells Mol Dis; 2021 Sep; 90():102587. PubMed ID: 34175765
[TBL] [Abstract][Full Text] [Related]
8. A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran.
Tajik S; Badalzadeh M; Fazlollahi MR; Houshmand M; Zandieh F; Khandan S; Pourpak Z
Iran J Allergy Asthma Immunol; 2016 Oct; 15(5):426-429. PubMed ID: 27917630
[TBL] [Abstract][Full Text] [Related]
9. Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian Patients.
Kulkarni M; Hule G; de Boer M; van Leeuwen K; Kambli P; Aluri J; Gupta M; Dalvi A; Mhatre S; Taur P; Desai M; Madkaikar M
J Clin Immunol; 2018 Nov; 38(8):898-916. PubMed ID: 30470980
[TBL] [Abstract][Full Text] [Related]
10. Clinical, functional and genetic characterization of 16 patients suffering from chronic granulomatous disease variants - identification of 11 novel mutations in CYBB.
Mollin M; Beaumel S; Vigne B; Brault J; Roux-Buisson N; Rendu J; Barlogis V; Catho G; Dumeril C; Fouyssac F; Monnier D; Gandemer V; Revest M; Brion JP; Bost-Bru C; Jeziorski E; Eitenschenck L; Jarrasse C; Drillon Haus S; Houachée-Chardin M; Hancart M; Michel G; Bertrand Y; Plantaz D; Kelecic J; Traberg R; Kainulainen L; Fauré J; Fieschi F; Stasia MJ
Clin Exp Immunol; 2021 Feb; 203(2):247-266. PubMed ID: 32954498
[TBL] [Abstract][Full Text] [Related]
11. Molecular diagnosis of X-linked chronic granulomatous disease in Iran.
Teimourian S; Rezvani Z; Badalzadeh M; Kannengiesser C; Mansouri D; Movahedi M; Zomorodian E; Parvaneh N; Mamishi S; Pourpak Z; Moin M
Int J Hematol; 2008 May; 87(4):398-404. PubMed ID: 18322777
[TBL] [Abstract][Full Text] [Related]
12. Characterization of six novel mutations in the CYBB gene leading to different sub-types of X-linked chronic granulomatous disease.
Stasia MJ; Bordigoni P; Floret D; Brion JP; Bost-Bru C; Michel G; Gatel P; Durant-Vital D; Voelckel MA; Li XJ; Guillot M; Maquet E; Martel C; Morel F
Hum Genet; 2005 Jan; 116(1-2):72-82. PubMed ID: 15538631
[TBL] [Abstract][Full Text] [Related]
13. Diagnostic paradigm for evaluation of male patients with chronic granulomatous disease, based on the dihydrorhodamine 123 assay.
Jirapongsananuruk O; Malech HL; Kuhns DB; Niemela JE; Brown MR; Anderson-Cohen M; Fleisher TA
J Allergy Clin Immunol; 2003 Feb; 111(2):374-9. PubMed ID: 12589359
[TBL] [Abstract][Full Text] [Related]
14. Missense mutations in the gp91-phox gene encoding cytochrome b558 in patients with cytochrome b positive and negative X-linked chronic granulomatous disease.
Kaneda M; Sakuraba H; Ohtake A; Nishida A; Kiryu C; Kakinuma K
Blood; 1999 Mar; 93(6):2098-104. PubMed ID: 10068684
[TBL] [Abstract][Full Text] [Related]
15. Mutations of chronic granulomatous disease in Turkish families.
Köker MY; Sanal O; De Boer M; Tezcan I; Metin A; Ersoy F; Roos D
Eur J Clin Invest; 2007 Jul; 37(7):589-95. PubMed ID: 17576211
[TBL] [Abstract][Full Text] [Related]
16. Genetic analysis of CYBB gene in 26 korean families with X-linked chronic granulomatous disease.
Ko SH; Rhim JW; Shin KS; Hahn YS; Lee SY; Kim JG
Immunol Invest; 2014; 43(6):585-94. PubMed ID: 24999735
[TBL] [Abstract][Full Text] [Related]
17. Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients.
Köker MY; Camcıoğlu Y; van Leeuwen K; Kılıç SŞ; Barlan I; Yılmaz M; Metin A; de Boer M; Avcılar H; Patıroğlu T; Yıldıran A; Yeğin O; Tezcan I; Sanal Ö; Roos D
J Allergy Clin Immunol; 2013 Nov; 132(5):1156-1163.e5. PubMed ID: 23910690
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel mutation in CYBB gene in a Chinese neonate with X-linked chronic granulomatous disease: A case report.
Zhang J; Fan M; Chen M; Wang H; Miao N; Yu H; Zhang L; Deng Q; Yi C
Medicine (Baltimore); 2022 Mar; 101(10):e28875. PubMed ID: 35451380
[TBL] [Abstract][Full Text] [Related]
19. [Report of a new mutation in CYBB gene in two patients with X linked chronic granulomatous disease].
Agudelo-Flórez P; Navarro S; Luttges P; López JA; Norambuena X; Navarrete S CL; Quezada A; Spencer M; Condino-Neto A; Cornejo de M
Rev Med Chil; 2006 Aug; 134(8):965-72. PubMed ID: 17130983
[TBL] [Abstract][Full Text] [Related]
20. CYBB mutation analysis in X-linked chronic granulomatous disease.
Jirapongsananuruk O; Niemela JE; Malech HL; Fleisher TA
Clin Immunol; 2002 Jul; 104(1):73-6. PubMed ID: 12139950
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
