144 related articles for article (PubMed ID: 35066806)
1. Upshaw-Schulman Syndrome with a Novel Deletion in Exon 17 of ADAMTS 13 Gene.
John BM; Kumar S; Saxena A
Indian J Pediatr; 2022 Apr; 89(4):402-403. PubMed ID: 35066806
[TBL] [Abstract][Full Text] [Related]
2. Upshaw-Schulman Syndrome With c.2728C>T Mutation in ADAMTS13 Gene.
Resham S; Fadoo Z; Moiz B
J Pediatr Hematol Oncol; 2019 Jan; 41(1):e60-e62. PubMed ID: 29771863
[TBL] [Abstract][Full Text] [Related]
3. [Siblings with congenital thrombotic thrombocytopenic purpura].
Funakoshi Y; Okada M; Matsumoto M; Kokame K; Moriuchi H
Rinsho Ketsueki; 2017; 58(8):933-937. PubMed ID: 28883277
[TBL] [Abstract][Full Text] [Related]
4. Congenital thrombotic thrombocytopenic purpura: Upshaw-Schulman syndrome: a cause of neonatal death and review of literature.
Sharma D; Shastri S; Pandita A; Sharma P
J Matern Fetal Neonatal Med; 2016; 29(12):1977-9. PubMed ID: 26365135
[TBL] [Abstract][Full Text] [Related]
5. Inherited thrombotic thrombocytopenic purpura in pregnancy.
Drews K; Seremak-Mrozikiewicz A; Sobieszczyk S; Barlik M
Neuro Endocrinol Lett; 2013; 34(6):508-13. PubMed ID: 24378452
[TBL] [Abstract][Full Text] [Related]
6. Two novel heterozygote missense mutations of the ADAMTS13 gene in a child with recurrent thrombotic thrombocytopenic purpura.
Rossio R; Ferrari B; Cairo A; Mancini I; Pisapia G; Palazzo G; Peyvandi F
Blood Transfus; 2013 Apr; 11(2):241-4. PubMed ID: 23058857
[TBL] [Abstract][Full Text] [Related]
7. Risk of diagnostic delay in congenital thrombotic thrombocytopenic purpura.
Ferrari B; Cairo A; Pagliari MT; Mancini I; Arcudi S; Peyvandi F
J Thromb Haemost; 2019 Apr; 17(4):666-669. PubMed ID: 30762934
[TBL] [Abstract][Full Text] [Related]
8. High prevalence of hereditary thrombotic thrombocytopenic purpura in central Norway: from clinical observation to evidence.
von Krogh AS; Quist-Paulsen P; Waage A; Langseth ØO; Thorstensen K; Brudevold R; Tjønnfjord GE; Largiadèr CR; Lämmle B; Kremer Hovinga JA
J Thromb Haemost; 2016 Jan; 14(1):73-82. PubMed ID: 26566785
[TBL] [Abstract][Full Text] [Related]
9. [Advance in the diagnosis and treatment of hereditary thrombotic thrombocytopenic purpura].
Liu W; Xiao Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Apr; 39(4):442-446. PubMed ID: 35446985
[TBL] [Abstract][Full Text] [Related]
10. A novel homozygous frameshift mutation in Exon 7 of the ADAMTS13 gene in a patient with congenital thrombotic thrombocytopenic purpura from India: a case report.
Yadav S; Shetty S; Kulkarni B
Transfusion; 2017 Nov; 57(11):2712-2714. PubMed ID: 28833243
[TBL] [Abstract][Full Text] [Related]
11. Inherited thrombotic thrombocytopenic purpura mimicking immune thrombocytopenic purpura during pregnancy: a case report.
Romão de Souza V; Beatriz Cavalcante de Oliveira A; Maria Vanderlei A; Queiroz da Mota Silveira Aroucha A; Pontes Duarte B; Nunes Machado A; Netto Chaer L; Wanderley de Barros Correia C; da Conceição de Barros Correia M; Freire Hazin Costa M
J Med Case Rep; 2018 Jan; 12(1):15. PubMed ID: 29357939
[TBL] [Abstract][Full Text] [Related]
12. Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): a short review.
Pérez-Rodríguez A; Lourés E; Rodríguez-Trillo Á; Costa-Pinto J; García-Rivero A; Batlle-López A; Batlle J; López-Fernández MF
Thromb Res; 2014 Dec; 134(6):1171-5. PubMed ID: 25242241
[TBL] [Abstract][Full Text] [Related]
13. A successfully treated case of an acute presentation of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) with decreased ADAMTS13 during late stage of pregnancy.
Nonaka T; Yamaguchi M; Nishijima K; Moriyama M; Takakuwa K; Enomoto T
J Obstet Gynaecol Res; 2021 May; 47(5):1892-1897. PubMed ID: 33751717
[TBL] [Abstract][Full Text] [Related]
14. An ADAMTS13 mutation that causes hereditary thrombotic thrombocytopenic purpura: a case report and literature review.
Li P; Jiang J; Xi Q; Yang Z
BMC Med Genomics; 2021 Oct; 14(1):252. PubMed ID: 34702267
[TBL] [Abstract][Full Text] [Related]
15. Upshaw-Schulman syndrome revisited: a concept of congenital thrombotic thrombocytopenic purpura.
Kinoshita S; Yoshioka A; Park YD; Ishizashi H; Konno M; Funato M; Matsui T; Titani K; Yagi H; Matsumoto M; Fujimura Y
Int J Hematol; 2001 Jul; 74(1):101-8. PubMed ID: 11530798
[TBL] [Abstract][Full Text] [Related]
16. Successful kidney transplantation in a patient with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome).
Fattah H; Kumar D; George JN; Massey HD; King AL; Friedman KD; Gupta G
Transfusion; 2017 Dec; 57(12):3058-3062. PubMed ID: 28940540
[TBL] [Abstract][Full Text] [Related]
17. [Variety of thrombotic thrombocytopenic purpura clinical course in Polish family members with ADAMTS 13 gene mutation].
Hyla-Klekot L; Kucharska G; Słonka K
Pol Merkur Lekarski; 2013 Mar; 34(201):161-4. PubMed ID: 23700827
[TBL] [Abstract][Full Text] [Related]
18. Congenital thrombotic thrombocytopenic purpura caused by new compound heterozygous mutations of the ADAMTS13 gene.
Rank CU; Kremer Hovinga J; Taleghani MM; Lämmle B; Gøtze JP; Nielsen OJ
Eur J Haematol; 2014 Feb; 92(2):168-71. PubMed ID: 24033710
[TBL] [Abstract][Full Text] [Related]
19. Long term follow up of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) on hemodialysis for 19 years: a case report.
Mise K; Ubara Y; Matsumoto M; Sumida K; Hiramatsu R; Hasegawa E; Yamanouchi M; Hayami N; Suwabe T; Hoshino J; Sawa N; Ohashi K; Kokame K; Miyata T; Fujimura Y; Takaichi K
BMC Nephrol; 2013 Jul; 14():156. PubMed ID: 23870247
[TBL] [Abstract][Full Text] [Related]
20. Inherited ADMATS13 deficiency: When to evoke the in the newborn?
Kasdallah N; Ben Salem H; Kbaier H; Ouederni M; Blibech S; Douagi M
Tunis Med; 2017 Jan; 95(1):67-69. PubMed ID: 29327771
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
