150 related articles for article (PubMed ID: 25449952)
1. Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland.
Schubert S; Haas C; Bartsch C; Mirshekarnejad M; Kohrs S; Roettinger I; Grosshennig A; Stuhrmann M; Scholz C; Schmidtke J
Mol Cell Probes; 2015 Feb; 29(1):31-4. PubMed ID: 25449952
[TBL] [Abstract][Full Text] [Related]
2. Genetic investigation of the TSPYL1 gene in sudden infant death syndrome.
Hering R; Frade-Martinez R; Bajanowski T; Poets CF; Tschentscher F; Riess O
Genet Med; 2006 Jan; 8(1):55-8. PubMed ID: 16418600
[TBL] [Abstract][Full Text] [Related]
3. Sudden infant death with dysgenesis of the testes syndrome in a non-Amish infant: A case report.
Slater B; Glinton K; Dai H; Lay E; Karaviti L; Mizerik E; Murali CN; Lalani SR; Bacino CA; Rossetti LZ
Am J Med Genet A; 2020 Nov; 182(11):2751-2754. PubMed ID: 32885560
[TBL] [Abstract][Full Text] [Related]
4. Should TSPYL1 mutation screening be included in routine diagnostics of male idiopathic infertility?
Javaher P; Stuhrmann M; Wilke C; Frenzel E; Manukjan G; Grosshenig A; Dechend F; Schwaab E; Schmidtke J; Schubert S
Fertil Steril; 2012 Feb; 97(2):402-6. PubMed ID: 22137496
[TBL] [Abstract][Full Text] [Related]
5. Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.
Rand CM; Berry-Kravis EM; Zhou L; Fan W; Weese-Mayer DE
Pediatr Res; 2007 Aug; 62(2):180-2. PubMed ID: 17597646
[TBL] [Abstract][Full Text] [Related]
6. The sudden infant death syndrome gene: does it exist?
Opdal SH; Rognum TO
Pediatrics; 2004 Oct; 114(4):e506-12. PubMed ID: 15466077
[TBL] [Abstract][Full Text] [Related]
7. Epileptic encephalopathy as a new feature of the sudden infant death with dysgenesis of the testes syndrome caused by TSPYL1 variants.
Mazel B; Mallet D; Roucher-Boulez F; Signor CB; Bournez M; Darmency V; Bourgeois V; Poe C; El Khabbaz F; Vitobello A; Philippe C; Duffourd Y; Thauvin-Robinet C; Faivre L; Nambot S
Am J Med Genet A; 2022 Dec; 188(12):3540-3545. PubMed ID: 36082874
[TBL] [Abstract][Full Text] [Related]
8. Analysis of PAC1 receptor gene variants in Caucasian and African American infants dying of sudden infant death syndrome.
Barrett KT; Rodikova E; Weese-Mayer DE; Rand CM; Marazita ML; Cooper ME; Berry-Kravis EM; Bech-Hansen NT; Wilson RJ
Acta Paediatr; 2013 Dec; 102(12):e546-52. PubMed ID: 23981011
[TBL] [Abstract][Full Text] [Related]
9. Sodium/proton exchanger 3 (NHE3) and sudden infant death syndrome (SIDS).
Studer J; Bartsch C; Haas C
Int J Legal Med; 2014 Nov; 128(6):939-43. PubMed ID: 24590378
[TBL] [Abstract][Full Text] [Related]
10. Unravelling the disease mechanism for TSPYL1 deficiency.
Buyse G; Di Michele M; Wijgaerts A; Louwette S; Wittevrongel C; Thys C; Downes K; Ceulemans B; Van Esch H; Van Geet C; Freson K
Hum Mol Genet; 2020 Dec; 29(20):3431-3442. PubMed ID: 33075815
[TBL] [Abstract][Full Text] [Related]
11. Noncardiac genetic predisposition in sudden infant death syndrome.
Gray B; Tester DJ; Wong LC; Chanana P; Jaye A; Evans JM; Baruteau AE; Evans M; Fleming P; Jeffrey I; Cohen M; Tfelt-Hansen J; Simpson MA; Ackerman MJ; Behr ER
Genet Med; 2019 Mar; 21(3):641-649. PubMed ID: 30139991
[TBL] [Abstract][Full Text] [Related]
12. Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year review.
Evans A; Bagnall RD; Duflou J; Semsarian C
Hum Pathol; 2013 Sep; 44(9):1730-6. PubMed ID: 23623143
[TBL] [Abstract][Full Text] [Related]
13. Identification of novel polymorphisms in the glucokinase and glucose-6-phosphatase genes in infants who died suddenly and unexpectedly.
Forsyth L; Hume R; Howatson A; Busuttil A; Burchell A
J Mol Med (Berl); 2005 Aug; 83(8):610-8. PubMed ID: 15918042
[TBL] [Abstract][Full Text] [Related]
14. Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.
Wedekind H; Bajanowski T; Friederich P; Breithardt G; Wülfing T; Siebrands C; Engeland B; Mönnig G; Haverkamp W; Brinkmann B; Schulze-Bahr E
Int J Legal Med; 2006 May; 120(3):129-37. PubMed ID: 16012827
[TBL] [Abstract][Full Text] [Related]
15. Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
Tester DJ; Wong LCH; Chanana P; Gray B; Jaye A; Evans JM; Evans M; Fleming P; Jeffrey I; Cohen M; Tfelt-Hansen J; Simpson MA; Behr ER; Ackerman MJ
J Pediatr; 2018 Dec; 203():423-428.e11. PubMed ID: 30268395
[TBL] [Abstract][Full Text] [Related]
16. IL6 G-174C associated with sudden infant death syndrome in a Caucasian Australian cohort.
Moscovis SM; Gordon AE; Al Madani OM; Gleeson M; Scott RJ; Roberts-Thomson J; Hall ST; Weir DM; Busuttil A; Blackwell CC
Hum Immunol; 2006 Oct; 67(10):819-25. PubMed ID: 17055359
[TBL] [Abstract][Full Text] [Related]
17. Genetic variation in hepatic glucose-6-phosphatase system genes in cases of sudden infant death syndrome.
Forsyth L; Scott HM; Howatson A; Busuttil A; Hume R; Burchell A
J Pathol; 2007 May; 212(1):112-20. PubMed ID: 17354259
[TBL] [Abstract][Full Text] [Related]
18. A controlled study of the relationship between Bordetella pertussis infections and sudden unexpected deaths among German infants.
Heininger U; Kleemann WJ; Cherry JD;
Pediatrics; 2004 Jul; 114(1):e9-15. PubMed ID: 15231967
[TBL] [Abstract][Full Text] [Related]
19. Aquaporin-4 polymorphisms and brain/body weight ratio in sudden infant death syndrome (SIDS).
Studer J; Bartsch C; Haas C
Pediatr Res; 2014 Jul; 76(1):41-5. PubMed ID: 24727946
[TBL] [Abstract][Full Text] [Related]
20. Sudden infant death syndrome (SIDS) and polymorphisms in Monoamine oxidase A gene (MAOA): a revisit.
Groß M; Bajanowski T; Vennemann M; Poetsch M
Int J Legal Med; 2014 Jan; 128(1):43-9. PubMed ID: 24173666
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
