164 related articles for article (PubMed ID: 33411152)
1. Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades' Experience.
Benhsaien I; Ailal F; El Bakkouri J; Jeddane L; Ouair H; Admou B; Bouskraoui M; Hbibi M; Hida M; Amenzoui N; Jouhadi Z; El Hafidi N; Rada N; Benajiba N; Abilkassem R; Badou A; Bousfiha AA
J Clin Immunol; 2021 Apr; 41(3):631-638. PubMed ID: 33411152
[TBL] [Abstract][Full Text] [Related]
2. Cytometric analysis and clinical features in a Moroccan cohort with severe combined immunodeficiency.
El Allam A; El Fakihi S; Tahoune H; Sahmoudi K; Bousserhane H; Bakri Y; El Hafidi N; Seghrouchni F
Hum Antibodies; 2022; 30(2):67-77. PubMed ID: 35094990
[TBL] [Abstract][Full Text] [Related]
3. Severe combined immunodeficiency in Serbia and Montenegro between years 1986 and 2010: a single-center experience.
Pasic S; Vujic D; Veljković D; Slavkovic B; Mostarica-Stojkovic M; Minic P; Minic A; Ristic G; Giliani S; Villa A; Sobacchi C; Lilić D; Abinun M
J Clin Immunol; 2014 Apr; 34(3):304-8. PubMed ID: 24481607
[TBL] [Abstract][Full Text] [Related]
4. A Decade Experience on Severe Combined Immunodeficiency Phenotype in Oman, Bridging to Newborn Screening.
Al Sukaiti N; Ahmed K; Alshekaili J; Al Kindi M; Cook MC; Farsi TA
Front Immunol; 2020; 11():623199. PubMed ID: 33519828
[TBL] [Abstract][Full Text] [Related]
5. Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network.
Cirillo E; Cancrini C; Azzari C; Martino S; Martire B; Pession A; Tommasini A; Naviglio S; Finocchi A; Consolini R; Pierani P; D'Alba I; Putti MC; Marzollo A; Giardino G; Prencipe R; Esposito F; Grasso F; Scarselli A; Di Matteo G; Attardi E; Ricci S; Montin D; Specchia F; Barzaghi F; Cicalese MP; Quaremba G; Lougaris V; Giliani S; Locatelli F; Rossi P; Aiuti A; Badolato R; Plebani A; Pignata C
Front Immunol; 2019; 10():1908. PubMed ID: 31456805
[TBL] [Abstract][Full Text] [Related]
6. Newborn Screening for SCID and Other Severe Primary Immunodeficiency in the Polish-German Transborder Area: Experience From the First 14 Months of Collaboration.
Giżewska M; Durda K; Winter T; Ostrowska I; Ołtarzewski M; Klein J; Blankenstein O; Romanowska H; Krzywińska-Zdeb E; Patalan MF; Bartkowiak E; Szczerba N; Seiberling S; Birkenfeld B; Nauck M; von Bernuth H; Meisel C; Bernatowska EA; Walczak M; Pac M
Front Immunol; 2020; 11():1948. PubMed ID: 33178177
[TBL] [Abstract][Full Text] [Related]
7. Clinical, Laboratory, and Molecular Findings for 63 Patients With Severe Combined Immunodeficiency: A Decade´s Experience.
Fazlollahi MR; Pourpak Z; Hamidieh AA; Movahedi M; Houshmand M; Badalzadeh M; Nourizadeh M; Mahloujirad M; Arshi S; Nabavi M; Gharagozlou M; Khayatzadeh A; Dabbaghzade A; Atarod L; Zandieh F; Sadeghi Shabestary M; Mesdaghi M; Mohammadzadeh I; Mahdaviani SA; Eslamian MH; Pesaran F; Bahraminia E; Abolnezhadian F; Arij Z; Moin M
J Investig Allergol Clin Immunol; 2017; 27(5):299-304. PubMed ID: 28266921
[TBL] [Abstract][Full Text] [Related]
8. Clinical, Immunological, and Molecular Findings in 57 Patients With Severe Combined Immunodeficiency (SCID) From India.
Aluri J; Desai M; Gupta M; Dalvi A; Terance A; Rosenzweig SD; Stoddard JL; Niemela JE; Tamankar V; Mhatre S; Bargir U; Kulkarni M; Shah N; Aggarwal A; Lashkari HP; Krishna V; Govindaraj G; Kalra M; Madkaikar M
Front Immunol; 2019; 10():23. PubMed ID: 30778343
[TBL] [Abstract][Full Text] [Related]
9. From Severe Combined Immunodeficiency to Omenn syndrome after hematopoietic stem cell transplantation in a RAG1 deficient family.
Martinez-Martinez L; Vazquez-Ortiz M; Gonzalez-Santesteban C; Martin-Nalda A; Vicente A; Plaza AM; Badell I; Alsina L; de la Calle-Martin O
Pediatr Allergy Immunol; 2012 Nov; 23(7):660-6. PubMed ID: 22882342
[TBL] [Abstract][Full Text] [Related]
10. Clinical Features and HSCT Outcome for SCID in Turkey.
Ikinciogullari A; Cagdas D; Dogu F; Tugrul T; Karasu G; Haskologlu S; Aksoylar S; Uygun V; Kupesiz A; Yildiran A; Gursel O; Ates C; Elhan A; Kansoy S; Yesilipek A; Tezcan I;
J Clin Immunol; 2019 Apr; 39(3):316-323. PubMed ID: 30924026
[TBL] [Abstract][Full Text] [Related]
11. Newborn Screening for Severe Combined Immunodeficiency: 10-Year Experience at a Single Referral Center (2009-2018).
Thorsen J; Kolbert K; Joshi A; Baker M; Seroogy CM
J Clin Immunol; 2021 Apr; 41(3):595-602. PubMed ID: 33409868
[TBL] [Abstract][Full Text] [Related]
12. Consanguinity rate and delay in diagnosis in Turkish patients with combined immunodeficiencies: a single-center study.
Azarsiz E; Gulez N; Edeer Karaca N; Aksu G; Kutukculer N
J Clin Immunol; 2011 Feb; 31(1):106-11. PubMed ID: 20924659
[TBL] [Abstract][Full Text] [Related]
13. Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency.
Kutukculer N; Gulez N; Karaca NE; Aksu G; Berdeli A
Ital J Pediatr; 2012 Mar; 38():8. PubMed ID: 22424479
[TBL] [Abstract][Full Text] [Related]
14. T
Stepensky P; Keller B; Shamriz O; von Spee-Mayer C; Friedmann D; Shadur B; Unger S; Fuchs S; NaserEddin A; Rumman N; Amro S; Molho Pessach V; Abuzaitoun O; Somech R; Elpeleg O; Ehl S; Warnatz K
J Clin Immunol; 2018 May; 38(4):527-536. PubMed ID: 29948574
[TBL] [Abstract][Full Text] [Related]
15. A Large Cohort of RAG1/2-Deficient SCID Patients-Clinical, Immunological, and Prognostic Analysis.
Greenberg-Kushnir N; Lee YN; Simon AJ; Lev A; Marcus N; Abuzaitoun O; Somech R; Stauber T
J Clin Immunol; 2020 Jan; 40(1):211-222. PubMed ID: 31838659
[TBL] [Abstract][Full Text] [Related]
16. Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations.
Giardino G; Sharapova SO; Ciznar P; Dhalla F; Maragliano L; Radha Rama Devi A; Islamoglu C; Ikinciogullari A; Haskologlu S; Dogu F; Hanna-Wakim R; Dbaibo G; Chou J; Cirillo E; Borzacchiello C; Kreins AY; Worth A; Rota IA; Marques JG; Sayitoglu M; Firtina S; Mahdi M; Geha R; Neven B; Sousa AE; Benfenati F; Hollander GA; Davies EG; Pignata C
J Clin Immunol; 2021 May; 41(4):756-768. PubMed ID: 33464451
[TBL] [Abstract][Full Text] [Related]
17. ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome.
Cagdas D; Gur Cetinkaya P; Karaatmaca B; Esenboga S; Tan C; Yılmaz T; Gümüş E; Barış S; Kuşkonmaz B; Ozgur TT; Bali P; Santisteban I; Orhan D; Yüce A; Cetinkaya D; Boztug K; Hershfield M; Sanal O; Tezcan İ
J Clin Immunol; 2018 May; 38(4):484-493. PubMed ID: 29744787
[TBL] [Abstract][Full Text] [Related]
18. Whole-exome sequencing of T
El Hawary R; Meshaal S; Mauracher AA; Opitz L; Abd Elaziz D; Lotfy S; Eldash A; Boutros J; Galal N; Pachlopnik Schmid J; Elmarsafy A
Clin Exp Immunol; 2021 Mar; 203(3):448-457. PubMed ID: 33040328
[TBL] [Abstract][Full Text] [Related]
19. First report on the Moroccan registry of primary immunodeficiencies: 15 years of experience (1998-2012).
Bousfiha AA; Jeddane L; El Hafidi N; Benajiba N; Rada N; El Bakkouri J; Kili A; Benmiloud S; Benhsaien I; Faiz I; Maataoui O; Aadam Z; Aglaguel A; Baba LA; Jouhadi Z; Abilkassem R; Bouskraoui M; Hida M; Najib J; Alj HS; Ailal F;
J Clin Immunol; 2014 May; 34(4):459-68. PubMed ID: 24619622
[TBL] [Abstract][Full Text] [Related]
20. Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia.
Alsmadi O; Al-Ghonaium A; Al-Muhsen S; Arnaout R; Al-Dhekri H; Al-Saud B; Al-Kayal F; Al-Saud H; Al-Mousa H
BMC Med Genet; 2009 Nov; 10():116. PubMed ID: 19912631
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
