BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 36708766)

  • 1. Is Your Kid Actin Out? A Series of Six Patients With Inherited Actin-Related Protein 2/3 Complex Subunit 1B Deficiency and Review of the Literature.
    Vásquez-Echeverri E; Yamazaki-Nakashimada MA; Venegas Montoya E; Scheffler Mendoza SC; Castano-Jaramillo LM; Medina-Torres EA; González-Serrano ME; Espinosa-Navarro M; Bustamante Ogando JC; González-Villarreal MG; Ortega Cisneros M; Valencia Mayoral PF; Consuelo Sanchez A; Varela-Fascinetto G; Ramírez-Uribe RMN; Salazar Gálvez Y; Bonifaz Alonzo LC; Fuentes-Pananá EM; Gómez Hernández N; Rojas Maruri CM; Casanova JL; Espinosa-Padilla SE; Staines Boone AT; López-Velázquez G; Boisson B; Lugo Reyes SO
    J Allergy Clin Immunol Pract; 2023 Apr; 11(4):1261-1280.e8. PubMed ID: 36708766
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Case Report: DOCK8 Deficiency Without Hyper-IgE in a Child With a Large Deletion.
    Venegas-Montoya E; Staines-Boone AT; Sánchez-Sánchez LM; García-Campos JA; Córdova-Gurrola RA; Salazar-Galvez Y; Múzquiz-Zermeño D; González-Serrano ME; Lugo Reyes SO
    Front Pediatr; 2021; 9():635322. PubMed ID: 34195158
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait?
    Chiriaco M; Ursu GM; Amodio D; Cotugno N; Volpi S; Berardinelli F; Pizzi S; Cifaldi C; Zoccolillo M; Prigione I; Di Cesare S; Giancotta C; Anastasio E; Rivalta B; Pacillo L; Zangari P; Fiocchi AG; Diociaiuti A; Bruselles A; Pantaleoni F; Ciolfi A; D'Oria V; Palumbo G; Gattorno M; El Hachem M; de Villartay JP; Finocchi A; Palma P; Rossi P; Tartaglia M; Aiuti A; Antoccia A; Di Matteo G; Cancrini C
    Front Immunol; 2022; 13():919237. PubMed ID: 35967303
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical, immunological and molecular profiles of DOCK8 deficiency in six patients from a tertiary care centre in North India.
    Kumar Jindal A; Sil A; Aggarwal R; Tyagi R; Mondal S; Singh A; Barman P; Chawla S; Loganathan SK; Gupta K; Vinay K; Mahajan R; Saikia B; Kaur G; Sharma R; Saka R; Bhatia A; Sankhyan N; Pandiarajan V; Pilania R; Dhaliwal M; Sharma S; Vyas S; Suri D; Rawat A; Singh S
    Clin Exp Dermatol; 2024 Feb; 49(3):226-234. PubMed ID: 37815217
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency.
    Sefer AP; Abolhassani H; Ober F; Kayaoglu B; Bilgic Eltan S; Kara A; Erman B; Surucu Yilmaz N; Aydogmus C; Aydemir S; Charbonnier LM; Kolukisa B; Azizi G; Delavari S; Momen T; Aliyeva S; Kendir Demirkol Y; Tekin S; Kiykim A; Baser OF; Cokugras H; Gursel M; Karakoc-Aydiner E; Ozen A; Krappmann D; Chatila TA; Rezaei N; Baris S
    J Clin Immunol; 2022 Apr; 42(3):634-652. PubMed ID: 35079916
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Case Report: A Novel Synonymous ARPC1B Gene Mutation Causes a Syndrome of Combined Immunodeficiency, Asthma, and Allergy With Significant Intrafamilial Clinical Heterogeneity.
    Papadatou I; Marinakis N; Botsa E; Tzanoudaki M; Kanariou M; Orfanou I; Kanaka-Gantenbein C; Traeger-Synodinos J; Spoulou V
    Front Immunol; 2021; 12():634313. PubMed ID: 33679784
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical, immunological, and genetic description of a Mexican cohort of patients with DOCK8 deficiency.
    Liquidano-Perez E; Maza-Ramos G; Perez Arias BA; Lugo Reyes SO; Barragan Arevalo T; Solorzano-Morales SA; Venegas Montoya E; Staines-Boone AT; Guzmán Cotaya R; Okada S; Picard C; Patin E; Ramirez-Uribe N; Bustamante-Ogando JC; Scheffler-Mendoza SC; Yamazaki-Nakashimada MA; Saez-de-Ocariz M; Espinosa Padilla SE; Gonzalez-Serrano ME
    Pediatr Allergy Immunol; 2024 Feb; 35(2):e14073. PubMed ID: 38351896
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Diversity in Serine/Threonine Protein Kinase-4 Deficiency and Review of the Literature.
    Cagdas D; Halacli SO; Tan C; Esenboga S; Karaatmaca B; Cetinkaya PG; Balcı-Hayta B; Ayhan A; Uner A; Orhan D; Boztug K; Ozen S; Topaloglu R; Sanal O; Tezcan I
    J Allergy Clin Immunol Pract; 2021 Oct; 9(10):3752-3766.e4. PubMed ID: 34146746
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Description of a Novel Pathogenic Variant in the ARPC1B and a Severe Allergy in Two Infants.
    Zaveleta Martínez O; Fregoso-Zuñiga AE; Razo Requena C; Espinosa Padilla S; Blancas Galicia L
    Iran J Allergy Asthma Immunol; 2024 Feb; 23(1):122-126. PubMed ID: 38485907
    [TBL] [Abstract][Full Text] [Related]  

  • 10. DOCK8 mutation diagnosed using whole-exome sequencing of the dried blood spot-derived DNA: a case report of an Iraqi girl diagnosed in Japan.
    Al-Kzayer LFY; Al-Aradi HMH; Shigemura T; Sano K; Tanaka M; Hamada M; Ali KH; Aldaghir OM; Nakazawa Y; Okuno Y
    BMC Med Genet; 2019 Jun; 20(1):114. PubMed ID: 31242861
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical Profile of Hyper-IgE Syndrome in India.
    Saikia B; Rawat A; Minz RW; Suri D; Pandiarajan V; Jindal A; Sahu S; Karim A; Desai M; Taur PD; Pandrowala A; Gowri V; Madkaikar M; Dalvi A; Yadav RM; Lashkari HP; Raj R; Uppuluri R; Swaminathan VV; Bhattad S; Cyril G; Kumar H; Shukla A; Kalra M; Govindaraj G; Singh S
    Front Immunol; 2021; 12():626593. PubMed ID: 33717144
    [No Abstract]   [Full Text] [Related]  

  • 12. Eosinophilia and elevated IgE serum levels: a red flag: when your diagnosis is not a common atopic eczema or common allergy.
    Criado PR; Miot HA; Ianhez M
    Inflamm Res; 2023 Mar; 72(3):541-551. PubMed ID: 36637497
    [TBL] [Abstract][Full Text] [Related]  

  • 13. EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency.
    Schipp C; Schlütermann D; Hönscheid A; Nabhani S; Höll J; Oommen PT; Ginzel S; Fleckenstein B; Stork B; Borkhardt A; Stepensky P; Fischer U
    Front Immunol; 2018; 9():2400. PubMed ID: 30386345
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Diagnostic challenge in a series of eleven patients with hyper IgE syndromes.
    Yaakoubi R; Mekki N; Ben-Mustapha I; Ben-Khemis L; Bouaziz A; Ben Fraj I; Ammar J; Hamzaoui A; Turki H; Boussofara L; Denguezli M; Haddad S; Ouederni M; Bejaoui M; Chan KW; Lau YL; Mellouli F; Barbouche MR; Ben-Ali M
    Front Immunol; 2022; 13():1057679. PubMed ID: 36703986
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DOCK8 Deficiency Presenting as an IPEX-Like Disorder.
    Alroqi FJ; Charbonnier LM; Keles S; Ghandour F; Mouawad P; Sabouneh R; Mohammed R; Almutairi A; Chou J; Massaad MJ; Geha RS; Baz Z; Chatila TA
    J Clin Immunol; 2017 Nov; 37(8):811-819. PubMed ID: 29058101
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel CARMIL2 (RLTPR) Mutation Presenting with Hyper-IgE and Eosinophilia: A Case Report.
    Zamani R; Zoghi S; Shahkarami S; Seyedpour S; Jimenez Heredia R; Boztug K; Rezaei N
    Endocr Metab Immune Disord Drug Targets; 2024; 24(5):596-605. PubMed ID: 37855284
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutation.
    Broides A; Mandola AB; Levy J; Yerushalmi B; Pinsk V; Eldan M; Shubinsky G; Hadad N; Levy R; Nahum A; Ben-Harosh M; Lev A; Simon A; Somech R
    Immunol Res; 2017 Jun; 65(3):651-657. PubMed ID: 28070732
    [TBL] [Abstract][Full Text] [Related]  

  • 18. DOCK8 deficiency: Insights into pathophysiology, clinical features and management.
    Biggs CM; Keles S; Chatila TA
    Clin Immunol; 2017 Aug; 181():75-82. PubMed ID: 28625885
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Severe atopy and allergy--rare hyper-IgE syndrome caused by the DOCK8 mutation as underlying condition].
    Koskenvuo M; Kainulainen L; Vanto T; Lukkarinen H; Lähteenmäki P; Ruuskanen O
    Duodecim; 2015; 131(6):541-4. PubMed ID: 26237897
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.