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Page 1
Showing results for ivemark s
Search for Avemarg S instead (1 results)
Renal-hepatic-pancreatic dysplasia syndrome (Ivemark's syndrome).
Vankalakunti M, Gupta K, Kakkar N, Das A. Vankalakunti M, et al. Diagn Pathol. 2007 Jul 2;2:24. doi: 10.1186/1746-1596-2-24. Diagn Pathol. 2007. PMID: 17605805 Free PMC article.
BACKGROUND: Renal-Hepatic-Pancreatic dysplasia syndrome described by Ivemark in 1959 constitutes a triad pancreatic fibrosis, renal dysplasia and hepatic dysgenesis. ...
BACKGROUND: Renal-Hepatic-Pancreatic dysplasia syndrome described by Ivemark in 1959 constitutes a triad pancreatic fibrosis, renal d …
[Ivemark's syndrome].
Takashima C. Takashima C. Rinsho Hoshasen. 1974 Oct;19(10):823-4. Rinsho Hoshasen. 1974. PMID: 4474497 Japanese. No abstract available.
[Ivemark's syndrome].
Brunelli L, Grampa G, Marra S. Brunelli L, et al. Minerva Pediatr. 1975 Apr 7;27(12):692-8. Minerva Pediatr. 1975. PMID: 1128469 Italian. No abstract available.
[Ivemark's syndrome: asplenia].
DAGENAIS-PERUSSE P, BARIL E, PILIC I, ROUX R. DAGENAIS-PERUSSE P, et al. Union Med Can. 1963 Aug;92:892-4. Union Med Can. 1963. PMID: 14024595 French. No abstract available.
Neonatal Assessment of Infants with Heterotaxy.
Geddes GC, Samudrala SS, Earing MG. Geddes GC, et al. Clin Perinatol. 2020 Mar;47(1):171-182. doi: 10.1016/j.clp.2019.10.011. Epub 2019 Oct 31. Clin Perinatol. 2020. PMID: 32000924 Review.
Bi-allelic pathogenic variations in DNAJB11 cause Ivemark II syndrome, a renal-hepatic-pancreatic dysplasia.
Jordan P, Arrondel C, Bessières B, Tessier A, Attié-Bitach T, Guterman S, Morinière V, Antignac C, Saunier S, Gubler MC, Heidet L. Jordan P, et al. Kidney Int. 2021 Feb;99(2):405-409. doi: 10.1016/j.kint.2020.09.029. Epub 2020 Oct 28. Kidney Int. 2021. PMID: 33129895
Here we show that biallelic pathogenic variations in DNAJB11 lead to a severe fetal disease including enlarged cystic kidneys, dilation and proliferation of pancreatic duct cells, and liver ductal plate malformation, an association known as Ivemark II syndrome. Cysts of th …
Here we show that biallelic pathogenic variations in DNAJB11 lead to a severe fetal disease including enlarged cystic kidneys, dilation and …
[Ivemark's syndrome (author's transl)].
Reuss M, Wilker D. Reuss M, et al. Z Kardiol. 1980 Jul;69(7):499-503. Z Kardiol. 1980. PMID: 7445649 German.
Following a case report of a newborn with Ivemark's syndrome, we go into etiology, embryology, and anatomy of this congenital cardiovascular disease with asplenia and other visceral abnormalities. ...
Following a case report of a newborn with Ivemark's syndrome, we go into etiology, embryology, and anatomy of this congenital …
Ivemark syndrome: bronchial compression from anomalous pulmonary venous anatomy.
Patel PH, Hayden J, Richardson R. Patel PH, et al. J Surg Case Rep. 2017 Mar 17;2017(3):rjx045. doi: 10.1093/jscr/rjx045. eCollection 2017 Mar. J Surg Case Rep. 2017. PMID: 28458851 Free PMC article.
Ivemark syndrome is a heterotaxy syndrome which affects multiple organs and affects roughly 1 in every 6000 deliveries. ...
Ivemark syndrome is a heterotaxy syndrome which affects multiple organs and affects roughly 1 in every 6000 deliveries. ...
Cardiac and Non-Cardiac Abnormalities in Heterotaxy Syndrome.
Mishra S. Mishra S. Indian J Pediatr. 2015 Dec;82(12):1135-46. doi: 10.1007/s12098-015-1925-x. Epub 2015 Nov 26. Indian J Pediatr. 2015. PMID: 26612104 Review.
Thoraco-abdominal viscera have unique morphological asymmetry, unlike the body's external organs. Heterotaxy syndrome is a disorder in which there is a loss of normal left to right asymmetry of thoraco-abdominal viscera and their naturally proscribed spatial relationship. …
Thoraco-abdominal viscera have unique morphological asymmetry, unlike the body's external organs. Heterotaxy syndrome is a disorder i …
[Ivemark's syndrome (spleen agenesia-syndrome)].
Féaux de Lacroix W, Mennicken U, Hering I, Fischer R. Féaux de Lacroix W, et al. Med Welt. 1971 Jul 10;27:1109-12. Med Welt. 1971. PMID: 5559660 German. No abstract available.
76 results