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Journal Abstract Search

128 related items for PubMed ID: 25712599

  • 1. 3-C Ritscher-Schinzel syndrome with spinal subarachnoid cyst.
    Sargar KM, Radmanesh A, Herman TE, Siegel MJ.
    J Perinatol; 2015 Mar; 35(3):233-4. PubMed ID: 25712599
    [No Abstract] [Full Text] [Related]

  • 2. Ritscher-Schinzel cranio-cerebello-cardiac syndrome.
    Herman TE, Siegel MJ.
    J Perinatol; 2008 Oct; 28(10):715-8. PubMed ID: 18825150
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  • 4. A preterm infant with prolonged respiratory problems due to Ritscher-Schinzel syndrome.
    Yurttutan S, Oncel MY, Yurttutan N, Altug N, Erdeve O, Dilmen U.
    Genet Couns; 2012 Oct; 23(3):383-7. PubMed ID: 23072186
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  • 8. [A phenotypic description of 26 patients with Ritscher-Schinzel syndrome (cranio-cerebello-cardiac dysplasia or 3C syndrome)].
    Pira-Paredes SM, Montoya-Villada JH, Franco-Restrepo JL, Moncada-Velez M, Cornejo JW.
    Rev Neurol; 2017 Jun 01; 64(11):481-488. PubMed ID: 28555453
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  • 9. Arachnoid cyst and costovertebral defects in Aicardi syndrome.
    Yüksel D, Yilmaz D, Usak E, Senbil N, Gürer Y.
    J Paediatr Child Health; 2009 Jun 01; 45(6):391-2. PubMed ID: 22530764
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  • 10. 3C syndrome with cryptorchidism and posterior embryotoxon.
    Papadopoulou E, Sifakis S, Rogalidou M, Makrigiannakis A, Giannakopoulou C, Petersen MB.
    Clin Dysmorphol; 2005 Apr 01; 14(2):97-100. PubMed ID: 15770133
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  • 11. [Ritscher-Schinzel syndrome caused by CCDC22 gene mutation: a case report].
    Liang YT, Jiang HY, Fu HY.
    Zhongguo Dang Dai Er Ke Za Zhi; 2020 Oct 01; 22(10):1135-1137. PubMed ID: 33059814
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  • 12. Ritscher-Schinzel (3C) syndrome: documentation of the phenotype.
    Kosaki K, Curry CJ, Roeder E, Jones KL.
    Am J Med Genet; 1997 Feb 11; 68(4):421-7. PubMed ID: 9021015
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  • 13. Ritscher-Schinzel (cranio-cerebello-cardiac, 3C) syndrome: report of four new cases with renal involvement.
    Seidahmed MZ, Alkuraya FS, Shaheed M, Al Zahrani M, Al Manea W, Mansour F, Mustafa T, Farid G, Salih MA.
    Am J Med Genet A; 2011 Jun 11; 155A(6):1393-7. PubMed ID: 21567916
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  • 17. Atrioventricular septal defect and tetralogy of Fallot: a 15-year experience.
    Anderson RH.
    Eur J Cardiothorac Surg; 1998 Jan 11; 13(1):109-10. PubMed ID: 9504743
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  • 19. Tetralogy of Fallot in a patient with Killian-Pallister syndrome.
    Grech V, Parascandalo R, Cuschieri A.
    Pediatr Cardiol; 1999 Jan 11; 20(2):134-5. PubMed ID: 9986890
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  • 20. Biallelic VPS35L pathogenic variants cause 3C/Ritscher-Schinzel-like syndrome through dysfunction of retriever complex.
    Kato K, Oka Y, Muramatsu H, Vasilev FF, Otomo T, Oishi H, Kawano Y, Kidokoro H, Nakazawa Y, Ogi T, Takahashi Y, Saitoh S.
    J Med Genet; 2020 Apr 11; 57(4):245-253. PubMed ID: 31712251
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