These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 32555393)

  • 21. Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patients.
    Arboleda H; Quintero L; Yunis E
    J Med Genet; 1997 May; 34(5):433-7. PubMed ID: 9152846
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome.
    Schrauwen I; Szelinger S; Siniard AL; Kurdoglu A; Corneveaux JJ; Malenica I; Richholt R; Van Camp G; De Both M; Swaminathan S; Turk M; Ramsey K; Craig DW; Narayanan V; Huentelman MJ
    PLoS One; 2015; 10(7):e0131797. PubMed ID: 26176221
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Anesthesia in an Aging Infant: Neonatal Progeroid Syndrome.
    Sahay N; Bhalotra A; Saini G; Dhanda A
    A A Case Rep; 2015 Nov; 5(10):173-5. PubMed ID: 26422454
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The Wiedemann-Rautenstrauch neonatal progeroid syndrome: a case report and review of the literature.
    Bitoun P; Lachassine E; Sellier N; Sauvion S; Gaudelus J
    Clin Dysmorphol; 1995 Jul; 4(3):239-45. PubMed ID: 7551161
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations at the 3' end of FBN1 gene.
    Jacquinet A; Verloes A; Callewaert B; Coremans C; Coucke P; de Paepe A; Kornak U; Lebrun F; Lombet J; Piérard GE; Robinson PN; Symoens S; Van Maldergem L; Debray FG
    Eur J Med Genet; 2014 Apr; 57(5):230-4. PubMed ID: 24613577
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Ophthalmic manifestations in a case of Wiedemann-Rautenstrauch syndrome.
    Barkley MR; O'Hagan SB
    J AAPOS; 2015 Dec; 19(6):559-61. PubMed ID: 26691040
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Transient progeroid phenotype and lipodystrophy in mosaic polyploidy.
    Kárteszi J; Kosztolányi G; Czakó M; Hadzsiev K; Morava É
    Clin Dysmorphol; 2006 Jan; 15(1):29-31. PubMed ID: 16317304
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A Case of Wiedemann-Rautenstrauch Syndrome With Fatal Hyperkalemic Renal Faliure.
    Ghamry MA; Salah R; Galal EI; Henin S; Dobs M
    Cureus; 2022 Sep; 14(9):e29320. PubMed ID: 36159344
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-gene.
    Graul-Neumann LM; Kienitz T; Robinson PN; Baasanjav S; Karow B; Gillessen-Kaesbach G; Fahsold R; Schmidt H; Hoffmann K; Passarge E
    Am J Med Genet A; 2010 Nov; 152A(11):2749-55. PubMed ID: 20979188
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Pathophysiology of premature aging characteristics in Mendelian progeroid disorders.
    Hennekam RCM
    Eur J Med Genet; 2020 Nov; 63(11):104028. PubMed ID: 32791128
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A synonymous variant contributes to a rare Wiedemann-Rautenstrauch syndrome complicated with mild anemia
    Peng Q; Zhang Y; Xian B; Wu L; Ding J; Ding W; Zhang X; Ding B; Li D; Wu J; Hu X; Lu G
    Front Mol Neurosci; 2022; 15():1026530. PubMed ID: 36385762
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Natural course of neonatal progeroid syndrome.
    Hou JW
    Pediatr Neonatol; 2009 Jun; 50(3):102-9. PubMed ID: 19579756
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Exome sequencing reveals a de novo POLD1 mutation causing phenotypic variability in mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome (MDPL).
    Elouej S; Beleza-Meireles A; Caswell R; Colclough K; Ellard S; Desvignes JP; Béroud C; Lévy N; Mohammed S; De Sandre-Giovannoli A
    Metabolism; 2017 Jun; 71():213-225. PubMed ID: 28521875
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Wiedemann-Rautenstrauch syndrome: first Indian case.
    Pandey M; Gupta N; Kabra M; Kumar A; Datta V; Saili A
    Indian J Pediatr; 2011 Dec; 78(12):1552-5. PubMed ID: 21630068
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A probable case of Wiedemann-Rautenstrauch syndrome or neonatal progeroid syndrome and review of the literature.
    Courtens W; Nuytinck L; Fricx C; André J; Vamos E
    Clin Dysmorphol; 1997 Jul; 6(3):219-27. PubMed ID: 9220191
    [TBL] [Abstract][Full Text] [Related]  

  • 36. POLR3A variants with striatal involvement and extrapyramidal movement disorder.
    Harting I; Al-Saady M; Krägeloh-Mann I; Bley A; Hempel M; Bierhals T; Karch S; Moog U; Bernard G; Huntsman R; van Spaendonk RML; Vreeburg M; Rodríguez-Palmero A; Pujol A; van der Knaap MS; Pouwels PJW; Wolf NI
    Neurogenetics; 2020 Apr; 21(2):121-133. PubMed ID: 31940116
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A progeroid syndrome with neonatal presentation and long survival maps to 19p13.3p13.2.
    Akawi N; Ali B; Al Gazali L
    Birth Defects Res A Clin Mol Teratol; 2013 Jul; 97(7):456-62. PubMed ID: 23696134
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Absence of Lamin A/C gene mutations in four Wiedemann-Rautenstrauch syndrome patients.
    Morales LC; Arboleda G; Rodríguez Y; Forero DA; Ramírez N; Yunis JJ; Arboleda H
    Am J Med Genet A; 2009 Dec; 149A(12):2695-9. PubMed ID: 19938095
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Report of a patient with consanguineous parents.
    Devos EA; Leroy JG; Frijns JP; Van den Berghe H
    Eur J Pediatr; 1981 Jul; 136(3):245-8. PubMed ID: 7262096
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Kyphoscoliosis in Wiedemann-Rautenstrauch-syndrome (neonatal progeroid syndrome)].
    Thorey F; Jäger M; Seller K; Krauspe R; Wild A
    Z Orthop Ihre Grenzgeb; 2003; 141(3):341-4. PubMed ID: 12822084
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.