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 *

148 related articles for article (PubMed ID: 15636261)

  • 1. [MCA/MR anomaly--case report].
    Mrugacz M; Sredzińska-Kita D; Bakunowicz-Lazarczyk A; Urban B
    Klin Oczna; 2004; 106(3 Suppl):538-9. PubMed ID: 15636261
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Cohen syndrome: report of a case.
    Naritomi K; Chinen Y
    Jpn J Hum Genet; 1997 Sep; 42(3):457-9. PubMed ID: 12503195
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).
    Fryns JP; Kleczkowska A; Smeets E; Thiry P; Geutjens J; Van den Berghe H
    Am J Med Genet; 1990 Dec; 37(4):546-7. PubMed ID: 2260606
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Cohen syndrome. A new case and review of the literature].
    Calzolari S; Ballardini M; De Marco P
    Minerva Pediatr; 1995 Mar; 47(3):83-7. PubMed ID: 7791717
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A familial syndrome with hypotonia, mental retardation and dysmorphic features resembling Cohen syndrome.
    Mejía-Baltodano G; Bobadilla L; Solís A; Mendoza R; Díaz-Gallardo MY; Barros-Núñez P
    Genet Couns; 1997; 8(4):311-6. PubMed ID: 9457500
    [TBL] [Abstract][Full Text] [Related]  

  • 6. KBG syndrome: review of the literature and findings of 5 affected patients.
    Kumar H; Prabhu N; Cameron A
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Sep; 108(3):e72-9. PubMed ID: 19716495
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Flecked-retina syndromes.
    Walia S; Fishman GA; Kapur R
    Ophthalmic Genet; 2009 Jun; 30(2):69-75. PubMed ID: 19373677
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Cohen syndrome.
    Fryns JP; Van den Berghe H
    J Genet Hum; 1981 Dec; 29(4):449-53. PubMed ID: 7328419
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mental retardation, hypotonia, obesity, ocular, facial, dental, and limb abnormalities (Cohen syndrome). Report of three patients.
    Goecke T; Majewski F; Kauther KD; Sterzel U
    Eur J Pediatr; 1982 Jul; 138(4):338-40. PubMed ID: 7128643
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Cohen syndrome].
    Kayashima T; Niikawa N
    Ryoikibetsu Shokogun Shirizu; 2001; (36):477-8. PubMed ID: 11596442
    [No Abstract]   [Full Text] [Related]  

  • 11. [General anesthesia in Cohen syndrome. Report of a clinical case].
    Cavaliere F; Cormaci S; Cormaci M; Alberti A
    Minerva Anestesiol; 1995 Apr; 61(4):163-6. PubMed ID: 7675274
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Search for the best indicators for the presence of a VPS13B gene mutation and confirmation of diagnostic criteria in a series of 34 patients genotyped for suspected Cohen syndrome.
    El Chehadeh S; Aral B; Gigot N; Thauvin-Robinet C; Donzel A; Delrue MA; Lacombe D; David A; Burglen L; Philip N; Moncla A; Cormier-Daire V; Rio M; Edery P; Verloes A; Bonneau D; Afenjar A; Jacquette A; Heron D; Sarda P; Pinson L; Doray B; Vigneron J; Leheup B; Frances-Guidet AM; Dienne G; Holder M; Masurel-Paulet A; Huet F; Teyssier JR; Faivre L
    J Med Genet; 2010 Aug; 47(8):549-53. PubMed ID: 20656880
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Multiple evanescent white-dot syndrome--case report].
    Zaczek-Zakrzewska K
    Klin Oczna; 2009; 111(4-6):149-52. PubMed ID: 19673447
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and ocular findings in the Brachmann-de Lange syndrome.
    Bowling EL; Spurlock DR; Sydnor CW; Teichmiller CD; Wesson MD
    J Am Optom Assoc; 1990 Jul; 61(7):527-32. PubMed ID: 2380471
    [TBL] [Abstract][Full Text] [Related]  

  • 15. New MCA/MR syndrome with generalized hypotonia, congenital hydronephrosis, and characteristic face.
    Okamoto N; Matsumoto F; Shimada K; Satomura K
    Am J Med Genet; 1997 Jan; 68(3):347-9. PubMed ID: 9024570
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cohen syndrome with insulin resistance and seizure.
    Atabek ME; Keskin M; Kurtoğlu S; Kumandas S
    Pediatr Neurol; 2004 Jan; 30(1):61-3. PubMed ID: 14738954
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Filippi syndrome: a specific MCA/MR complex within the spectrum of so called "craniodigital syndromes". Report of an additional patient with a peculiar mpp and review of the literature.
    Franceschini P; Licata D; Guala A; Di Cara G; Franceschini D
    Genet Couns; 2002; 13(3):343-52. PubMed ID: 12416644
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Cohen's syndrome: non-causal association with vascular rings].
    Pérez-Caballero Macarrón C; Lozano Giménez C; Quintana Castilla A; Aparicio Meix JM
    An Esp Pediatr; 2000 Mar; 52(3):289-95. PubMed ID: 11003912
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The de Barsy syndrome.
    Arazi M; Kapicioğlu MI; Mutlu M
    Turk J Pediatr; 2001; 43(1):79-84. PubMed ID: 11297166
    [TBL] [Abstract][Full Text] [Related]  

  • 20. KBG syndrome.
    Brancati F; Sarkozy A; Dallapiccola B
    Orphanet J Rare Dis; 2006 Dec; 1():50. PubMed ID: 17163996
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.