124 related articles for article (PubMed ID: 19852434)
21. A Brazilian family with quadrupedal gait, severe mental retardation, coarse facial characteristics, and hirsutism.
Garcias Gde L; Roth Mda G
Int J Neurosci; 2007 Jul; 117(7):927-33. PubMed ID: 17613106
[TBL] [Abstract][Full Text] [Related]
22. An erythematous rash, diarrhea, failure to thrive, and lymphadenopathy in a 3-month-old girl.
Sicherer SH; Lederman HM
Ann Allergy Asthma Immunol; 1997 Mar; 78(3):253-8. PubMed ID: 9087148
[No Abstract] [Full Text] [Related]
23. Pediatric AIDS with severe T-cell depression and hypogammaglobulinemia.
Koutsonikolis A; Nelson RP; Kornfeld SJ; Day NK; Good RA
Clin Pediatr (Phila); 1995 Nov; 34(11):605-7. PubMed ID: 8565392
[No Abstract] [Full Text] [Related]
24. Toriello-Carey syndrome in a Turkish newborn.
Uras N; Sandal G; Oguz S; Aydemir O; Erdeve O; Dilmen U
Genet Couns; 2009; 20(3):243-7. PubMed ID: 19852430
[TBL] [Abstract][Full Text] [Related]
25. An Infant with Respiratory Distress and Loose Stools.
Reddy P; Laishram D; Jindal AK; Gupta K; Rawat A
Indian Pediatr; 2018 Aug; 55(8):693-697. PubMed ID: 30218520
[TBL] [Abstract][Full Text] [Related]
26. Dubowitz syndrome: a cholesterol metabolism disorder?
Yeşilkaya E; Karaer K; Bideci A; Camurdan O; Perçin EF; Cinaz P
Genet Couns; 2008; 19(3):287-90. PubMed ID: 18990984
[TBL] [Abstract][Full Text] [Related]
27. Adenosine deaminase deficiency can present with features of Omenn syndrome.
Roifman CM; Zhang J; Atkinson A; Grunebaum E; Mandel K
J Allergy Clin Immunol; 2008 Apr; 121(4):1056-8. PubMed ID: 18243287
[No Abstract] [Full Text] [Related]
28. ORAI1 defect in a patient with disseminated CMV infection and severe hypotonia.
Deveci K; Esenboğa S; Bildik HN; Ocak M; Gülşen HH; Ertuğrul İ; Oğuz KK; Çağdaş D; Yalnızoğlu D; Tezcan İ
Turk J Pediatr; 2023; 65(4):698-703. PubMed ID: 37661687
[TBL] [Abstract][Full Text] [Related]
29. A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency.
Firtina S; Cipe F; Ng YY; Kiykim A; Ng OH; Sudutan T; Aydogmus C; Baris S; Ozturk G; Aydiner E; Ozen A; Sayitoglu M
J Clin Immunol; 2019 Feb; 39(2):144-147. PubMed ID: 30903456
[No Abstract] [Full Text] [Related]
30. Signal transducer and activator of transcription 5 tyrosine phosphorylation for the diagnosis and monitoring of patients with severe combined immunodeficiency.
Walshe D; Gaspar HB; Thrasher AJ; Cale CM; Gilmour KC
J Allergy Clin Immunol; 2009 Feb; 123(2):505-8. PubMed ID: 19203666
[No Abstract] [Full Text] [Related]
31. Graves disease in an eight year old boy of Down Syndrome.
Ahluwalia AI; Narayan S
Indian Pediatr; 2005 Jan; 42(1):76-7. PubMed ID: 15695868
[No Abstract] [Full Text] [Related]
32. Posttransfusion graft-versus-host disease in an infant with severe combined immunodeficiency.
Rahiminejad MS; Kashef S
Transplant Proc; 2003 Nov; 35(7):2825-6. PubMed ID: 14612130
[No Abstract] [Full Text] [Related]
33. Hemophagocytic lymphohistiocytosis: when the immune system runs amok.
Janka G
Klin Padiatr; 2009 Sep; 221(5):278-85. PubMed ID: 19707989
[TBL] [Abstract][Full Text] [Related]
34. Left ventricular aneurysm in a child with severe combined immunodeficiency syndrome.
Jamshidi R; Hornberger LK; Karl TR
Ann Thorac Surg; 2009 Nov; 88(5):1678-80. PubMed ID: 19853138
[TBL] [Abstract][Full Text] [Related]
35. A 1-month-old boy with jaundice, thrush, and respiratory distress.
Barone MA; Lederman HM
Curr Opin Pediatr; 1994 Dec; 6(6):682-6. PubMed ID: 7849814
[No Abstract] [Full Text] [Related]
36. [X-linked severe combined immunodeficiency].
Kumaki S
Nihon Rinsho Meneki Gakkai Kaishi; 2002 Feb; 25(1):140-5. PubMed ID: 11963175
[No Abstract] [Full Text] [Related]
37. Severe combined immunodeficiency.
Shah I
Indian Pediatr; 2005 Aug; 42(8):819-22. PubMed ID: 16141485
[No Abstract] [Full Text] [Related]
38. Genetic mosaicism: what Gregor Mendel didn't know.
Hirschhorn R
J Clin Invest; 1995 Feb; 95(2):443-4. PubMed ID: 7860724
[No Abstract] [Full Text] [Related]
39. Extensive tinea in a patient with severe combined immunodeficiency.
Jiménez-Puya R; Vázquez-Bayo C; Rodriguez-Bujaldón A; Gómez García F; Moreno-Giménez JC
Pediatr Dermatol; 2009; 26(2):213-4. PubMed ID: 19419475
[TBL] [Abstract][Full Text] [Related]
40. A case of a bloodstained amniotic fluid sample from a pregnant woman with Down syndrome analyzed by QF-PCR after low-speed centrifugation.
Andonova S; Dimitrova V; Boneva I; Kremensky I
Prenat Diagn; 2008 May; 28(5):457-9. PubMed ID: 18438959
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]