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3. JAK inhibition in early-onset somatic, nonclonal STAT5B gain-of-function disease. Eisenberg R; Gans MD; Leahy TR; Gothe F; Perry C; Raffeld M; Xi L; Blackstone S; Ma C; Hambleton S; Milner JD J Allergy Clin Immunol Pract; 2021 Feb; 9(2):1008-1010.e2. PubMed ID: 33290916 [No Abstract] [Full Text] [Related]
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5. [Muckle-Wells syndrome: a new familial case. Demonstration of abnormalities of lymphocyte subpopulations]. Nicolas JF; Garnier JL; Marchand C; Thivolet J Ann Dermatol Venereol; 1989; 116(11):827-9. PubMed ID: 2619177 [No Abstract] [Full Text] [Related]
6. New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes. Dodé C; Le Dû N; Cuisset L; Letourneur F; Berthelot JM; Vaudour G; Meyrier A; Watts RA; Scott DG; Nicholls A; Granel B; Frances C; Garcier F; Edery P; Boulinguez S; Domergues JP; Delpech M; Grateau G Am J Hum Genet; 2002 Jun; 70(6):1498-506. PubMed ID: 11992256 [TBL] [Abstract][Full Text] [Related]
7. A novel gain-of-function mutation in STAT5B is associated with treatment-resistant severe atopic dermatitis. Kasap N; Aslan K; Karakurt LT; Bozkurt H; Canatan H; Cavkaytar O; Eken A; Arga M Clin Exp Allergy; 2022 Jul; 52(7):907-910. PubMed ID: 35426955 [No Abstract] [Full Text] [Related]
8. Treatment of hypereosinophilic syndrome and eosinophilic dermatitis with reslizumab. Kuruvilla M Ann Allergy Asthma Immunol; 2018 Jun; 120(6):670-671. PubMed ID: 29496465 [No Abstract] [Full Text] [Related]
9. Uncovering the pathogenesis of large granular lymphocytic leukemia-novel STAT3 and STAT5b mutations. Rajala HL; Porkka K; Maciejewski JP; Loughran TP; Mustjoki S Ann Med; 2014 May; 46(3):114-22. PubMed ID: 24512550 [TBL] [Abstract][Full Text] [Related]
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11. Human signal transducer and activator of transcription 5b (STAT5b) mutation causes dysregulated human natural killer cell maturation and impaired lytic function. Vargas-Hernández A; Witalisz-Siepracka A; Prchal-Murphy M; Klein K; Mahapatra S; Al-Herz W; Mace EM; Carisey AF; Orange JS; Sexl V; Forbes LR J Allergy Clin Immunol; 2020 Jan; 145(1):345-357.e9. PubMed ID: 31600547 [TBL] [Abstract][Full Text] [Related]
12. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings. Pugliese-Pires PN; Tonelli CA; Dora JM; Silva PC; Czepielewski M; Simoni G; Arnhold IJ; Jorge AA Eur J Endocrinol; 2010 Aug; 163(2):349-55. PubMed ID: 20538865 [TBL] [Abstract][Full Text] [Related]
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15. Long-term follow-up of STAT5B deficiency in three argentinian patients: clinical and immunological features. Bezrodnik L; Di Giovanni D; Caldirola MS; Azcoiti ME; Torgerson T; Gaillard MI J Clin Immunol; 2015 Apr; 35(3):264-72. PubMed ID: 25753012 [TBL] [Abstract][Full Text] [Related]
16. Growth hormone secretion and immunological function of a male patient with a homozygous STAT5b mutation. Walenkamp MJ; Vidarsdottir S; Pereira AM; Karperien M; van Doorn J; van Duyvenvoorde HA; Breuning MH; Roelfsema F; Kruithof MF; van Dissel J; Janssen R; Wit JM; Romijn JA Eur J Endocrinol; 2007 Feb; 156(2):155-65. PubMed ID: 17287404 [TBL] [Abstract][Full Text] [Related]
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