BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

105 related articles for article (PubMed ID: 7745379)

  • 1. Kenny-Caffe syndrome.
    Churesigaew S
    J Med Assoc Thai; 1994 Oct; 77(10):554-9. PubMed ID: 7745379
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Kenny-Caffey syndrome. Case report and literature review.
    Abdel-Al YK; Auger LT; el-Gharbawy F
    Clin Pediatr (Phila); 1989 Apr; 28(4):175-9. PubMed ID: 2649298
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ocular findings in Kenny's syndrome.
    Boynton JR; Pheasant TR; Johnson BL; Levin DB; Streeten BW
    Arch Ophthalmol; 1979 May; 97(5):896-900. PubMed ID: 444124
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Kenny-Caffey syndrome type 1 in an Egyptian girl.
    Metwalley KA; Farghaly HS
    Indian J Endocrinol Metab; 2012 Sep; 16(5):827-9. PubMed ID: 23087875
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of optical coherence topography findings in Kenny-Caffey syndrome.
    Timoney P; Darcy F; McCreery K; Reardon W; Brosnahan D
    J AAPOS; 2007 Jun; 11(3):291-3. PubMed ID: 17360206
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital medullary tubular stenosis. A case of Caffey-Kenny syndrome.
    Enriquez EJ; Toledo F; Bustamante-Cruz M; Cruz GM
    Acta Orthop Scand; 1988 Jun; 59(3):326-7. PubMed ID: 3381667
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital nephrotic syndrome presenting with cerebral venous thrombosis, hypocalcemia, and seizures in the neonatal period.
    Fofah O; Roth P
    J Perinatol; 1997; 17(6):492-4. PubMed ID: 9447540
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Kenny syndrome: case report and literature review.
    Tsai CE; Chiu PC; Lee ML
    J Formos Med Assoc; 1996 Oct; 95(10):793-7. PubMed ID: 8961678
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sanjad-Sakati syndrome/Kenny-Caffey syndrome type 1: a study of 21 cases in Kuwait.
    Naguib KK; Gouda SA; Elshafey A; Mohammed F; Bastaki L; Azab AS; Alawadi SA
    East Mediterr Health J; 2009; 15(2):345-52. PubMed ID: 19554981
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic variability of Pai syndrome: report of two patients and review of the literature.
    Vaccarella F; Pini Prato A; Fasciolo A; Pisano M; Carlini C; Seymandi PL
    Int J Oral Maxillofac Surg; 2008 Nov; 37(11):1059-64. PubMed ID: 18657395
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Further delineation of phenotype and genotype of Kenny-Caffey syndrome type 2 (phenotype and genotype of KCS type 2).
    Chen X; Zou C
    Mol Genet Genomic Med; 2024 Apr; 12(4):e2433. PubMed ID: 38591167
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Diaphyseal tubular stenosis (Kenny-Caffey syndrome), with hydrocephalus as an associated malformation].
    Rodríguez Costa T; Casas Fernández C; Puche Mira A; Castro García FJ; Mula García JA
    An Esp Pediatr; 1988 May; 28(5):474-6. PubMed ID: 3178069
    [No Abstract]   [Full Text] [Related]  

  • 13. Kabuki syndrome - report of six cases and review of the literature with emphasis on ocular features.
    Kluijt I; van Dorp DB; Kwee ML; Toutain A; Keppler-Noreuil K; Warburg M; Bitoun P
    Ophthalmic Genet; 2000 Mar; 21(1):51-61. PubMed ID: 10779849
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Kenny-Caffey Syndrome: oral findings and 4-year follow-up of overlay denture therapy.
    Demir T; Kecik D; Cehreli ZC
    J Dent Child (Chic); 2007; 74(3):236-40. PubMed ID: 18482522
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The ocular manifestations of Weissenbacher-Zweymuller syndrome.
    Rabinowitz R; Gradstein L; Galil A; Levy J; Lifshitz T
    Eye (Lond); 2004 Dec; 18(12):1258-63. PubMed ID: 15044941
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Compartment syndrome after hypocalcemic tetany: a case report.
    Luzzi R; Burghardt RD; Herzenberg JE; Zuckerberg AL
    J Pediatr Orthop; 2008 Sep; 28(6):688-90. PubMed ID: 18724210
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Parathyroid function and growth in 22q11.2 deletion syndrome.
    Brauner R; Le Harivel de Gonneville A; Kindermans C; Le Bidois J; Prieur M; Lyonnet S; Souberbielle JC
    J Pediatr; 2003 May; 142(5):504-8. PubMed ID: 12756381
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Disease progression in Hutchinson-Gilford progeria syndrome: impact on growth and development.
    Gordon LB; McCarten KM; Giobbie-Hurder A; Machan JT; Campbell SE; Berns SD; Kieran MW
    Pediatrics; 2007 Oct; 120(4):824-33. PubMed ID: 17908770
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Weaver syndrome with pes cavus.
    Farrell SA; Hughes HE
    Am J Med Genet; 1985 Aug; 21(4):737-9. PubMed ID: 4025398
    [TBL] [Abstract][Full Text] [Related]  

  • 20. SHORT syndrome: a case with high hyperopia and astigmatism.
    Bonnel S; Dureau P; LeMerrer M; Dufier JL
    Ophthalmic Genet; 2000 Dec; 21(4):235-8. PubMed ID: 11135494
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.