BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 17351360)

  • 1. Prader-Willi and Klinefelter syndrome: a coincidence or not?
    Vasudevan PC; Quarrell OWJ
    Clin Dysmorphol; 2007 Apr; 16(2):127-129. PubMed ID: 17351360
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Atypical presentation of Prader-Willi syndrome with Klinefelter (XXY karytype) and craniosynostosis.
    Carvalho DR; Trad CS; Pina-Neto JM
    Arq Neuropsiquiatr; 2006 Jun; 64(2A):303-5. PubMed ID: 16791374
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A 47, XXY patient and Xq21.31 duplication with features of Prader-Willi syndrome: results of array-based comparative genomic hybridization.
    Pramyothin P; Pithukpakorn M; Arakaki RF
    Endocrine; 2010 Jun; 37(3):379-82. PubMed ID: 20960156
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A further case of coincidental Prader-Willi and Klinefelter syndromes.
    Schneider M; Forrester S; Crain V; Kimonis V
    Am J Med Genet A; 2004 Apr; 126A(2):213-4. PubMed ID: 15057989
    [No Abstract]   [Full Text] [Related]  

  • 5. Further example of a patient with Prader-Willi and Klinefelter syndromes of different parental origins.
    Geffroy S; Evrard V; Taufour D; Vanderbecken S; de Martinville B
    Am J Med Genet; 1998 Nov; 80(3):286-7. PubMed ID: 9843055
    [No Abstract]   [Full Text] [Related]  

  • 6. A case with 47,XXY,del(15)(q11;q13) karyotype associated with Prader-Willi phenotype.
    Rego A; Coll MD; Regal M; Guitart M; Escudero T; García-Mayor RV
    Horm Res; 1997; 48(1):44-6. PubMed ID: 9195210
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosomal Aberrations with Endocrine Relevance (Turner Syndrome, Klinefelter Syndrome, Prader-Willi Syndrome).
    Haltrich I
    Exp Suppl; 2019; 111():443-473. PubMed ID: 31588543
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.
    Gunay-Aygun M; Schwartz S; Heeger S; O'Riordan MA; Cassidy SB
    Pediatrics; 2001 Nov; 108(5):E92. PubMed ID: 11694676
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Klinefelter and trisomy X syndromes in patients with Prader-Willi syndrome and uniparental maternal disomy of chromosome 15--a coincidence?
    Butler MG; Hedges LK; Rogan PK; Seip JR; Cassidy SB; Moeschler JB
    Am J Med Genet; 1997 Oct; 72(1):111-4. PubMed ID: 9295086
    [No Abstract]   [Full Text] [Related]  

  • 10. Congenital ocular fibrosis syndrome associated with the Prader-Willi syndrome.
    Kalpakian B; Bateman JB; Sparkes RS; Wood GK
    J Pediatr Ophthalmol Strabismus; 1986; 23(4):170-3. PubMed ID: 3746591
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Klinefelter's syndrome and Prader-Willi syndrome: a rare combination.
    Verhoeven WM; de Vries BB; Duffels SJ; Egger JI; Noordam C; Tuinier S
    Psychopathology; 2007; 40(5):356-60. PubMed ID: 17657135
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A 14-year-old male patient with diagnosis of Prader-Willi syndrome in Ethiopia: a case report.
    Belay KE; Ayalew BL; Amogne MT; Alemneh TA; Geletew TK
    J Med Case Rep; 2023 Dec; 17(1):530. PubMed ID: 38143282
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hypogonadism in Patients with Prader Willi Syndrome: A Narrative Review.
    Napolitano L; Barone B; Morra S; Celentano G; La Rocca R; Capece M; Morgera V; Turco C; Caputo VF; Spena G; Romano L; De Luca L; Califano G; Collà Ruvolo C; Mangiapia F; Mirone V; Longo N; Creta M
    Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33671467
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Prader-Labhart-Willi syndrome in infants].
    Schmeling H; Gillessen-Kaesbach G; Schulte-Mattler U; Burdach S; Horneff G
    Klin Padiatr; 2002; 214(2):51-3. PubMed ID: 11972309
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Xq21.31 duplication without features of Prader-Willi syndrome.
    Castro-Gago M; Pérez-Gay L; Gómez-Lado C; Barros-Angueira F
    Endocrine; 2013 Feb; 43(1):238. PubMed ID: 22763470
    [No Abstract]   [Full Text] [Related]  

  • 16. Prader-Willi syndrome: clinical and molecular cytogenetic investigations.
    Hou JW; Wang TR
    J Formos Med Assoc; 1996 Jun; 95(6):474-9. PubMed ID: 8772055
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neonatal presentation of Prader Willi sindrome. Personal records.
    Maggio MC; Corsello M; Piccione M; Piro E; Giuffrè M; Liotta A
    Minerva Pediatr; 2007 Dec; 59(6):817-23. PubMed ID: 17978792
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Multiorgan failure associated with hyperthermia in an infant with Prader-Willi syndrome. case report].
    Donoso A; Arriagada D; Campbell S; Cruces P
    Arch Argent Pediatr; 2013 Oct; 111(5):e117-20. PubMed ID: 24092035
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Diagnosis of Prader-Willi syndrome. Considerations on a case of erroneous diagnosis].
    Scommegna S; Zollino M; Paolone G
    Pediatr Med Chir; 2001; 23(3-4):191-6. PubMed ID: 11723857
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prader-Willi syndrome.
    Cassidy SB
    J Med Genet; 1997 Nov; 34(11):917-23. PubMed ID: 9391886
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.