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 *

485 related articles for article (PubMed ID: 8650457)

  • 41. Prader-Willi syndrome in a child with XYY.
    Honma A; Ishii R; Ito A; Kato M; Saitoh S; Hayasaka K
    J Hum Genet; 1999; 44(6):412-3. PubMed ID: 10570915
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Molecular diagnosis of Prader-Willi syndrome.
    Pangkanon S
    J Med Assoc Thai; 2003 Aug; 86 Suppl 3():S510-6. PubMed ID: 14700141
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Breathing abnormalities during sleep in Kleine-Levin Syndrome: fact or coincidence?
    Gadoth N
    Curr Opin Pulm Med; 2018 Jul; 24(4):403-405. PubMed ID: 29553974
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [The Prader-Willi syndrome. A diagnostic update].
    Vieto E; Ward J; Quetglas P
    Rev Med Panama; 1994 May; 19(2):101-5. PubMed ID: 7991800
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.
    D'Angelo CS; Da Paz JA; Kim CA; Bertola DR; Castro CI; Varela MC; Koiffmann CP
    Eur J Med Genet; 2006; 49(6):451-60. PubMed ID: 16564757
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Ocular findings in a patient with Prader-Willi syndrome.
    Wang XC; Norose K; Kiyosawa K; Segawa K
    Jpn J Ophthalmol; 1995; 39(3):284-9. PubMed ID: 8577080
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Aerodynamic and acoustic characteristics of voice in Prader-Willi syndrome.
    Defloor T; Van Borsel J; Curfs L; De Bodt M
    J Voice; 2001 Jun; 15(2):284-90. PubMed ID: 11411482
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Kleine-Levin-syndrome (author's transl)].
    Lenz H
    Wien Med Wochenschr; 1980 Jun; 130(11):373-5. PubMed ID: 6934661
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Kleine-Levin syndrome and bipolar disorder: a differential diagnosis of recurrent and resistant depression.
    Geoffroy PA; Arnulf I; Etain B; Henry C
    Bipolar Disord; 2013 Dec; 15(8):899-902. PubMed ID: 24034447
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15.
    Gunay-Aygun M; Heeger S; Schwartz S; Cassidy SB
    Am J Med Genet; 1997 Jul; 71(1):106-10. PubMed ID: 9215778
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Kleine Levin Syndrome: more than just periodic hypersomnia].
    Pillen S; Vandenbussche NL; Fronczek R; van Duijn J; Lammers GJ; Overeem S
    Ned Tijdschr Geneeskd; 2016; 160():D238. PubMed ID: 27484420
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [The hypotonia-hypomentia-hypogonadism-obesity syndrome (Prader-Willi-Labhart syndrome) in a 38-year-old man].
    van Bergeijk L; van der Veen EA
    Ned Tijdschr Geneeskd; 1980 Dec; 124(49):2090-2. PubMed ID: 7442851
    [No Abstract]   [Full Text] [Related]  

  • 53. Behavioral and psychiatric disorders in Prader-Willi syndrome: a population study in Japan.
    Hiraiwa R; Maegaki Y; Oka A; Ohno K
    Brain Dev; 2007 Oct; 29(9):535-42. PubMed ID: 17314021
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Neonatal hypotonia in Prader-Willi syndrome due to t(15;16)].
    Fernández-Novoa MC; Vargas MT; Santano MR; Moya J; Garnacho MC
    Rev Neurol; 2000 Sep 1-15; 31(5):499-500. PubMed ID: 11027108
    [No Abstract]   [Full Text] [Related]  

  • 55. Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.
    Engelen JJ; Loots WJ; Albrechts JC; Schrander-Stumpel CT; Dirckx R; Smeets HJ; Hamers AJ; Geraedts JP
    Genet Couns; 1999; 10(2):123-32. PubMed ID: 10422004
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant.
    Giurgiutiu DV; Espinoza LM; Wood TC; DuPont BR; Holden KR
    J Child Neurol; 2008 Jan; 23(1):112-7. PubMed ID: 18184946
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Apparent resolution of hypersomnia episodes in two patients with Kleine-Levin syndrome following treatment with the melatonin receptor agonist ramelteon.
    Dominguez D; Rudock R; Tomko S; Pathak S; Mignot E; Licis A
    J Clin Sleep Med; 2024 Apr; 20(4):657-662. PubMed ID: 38156412
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Prader-Willi syndrome: sorting out the relationships between obesity, hypersomnia, and sleep apnea.
    Bruni O; Verrillo E; Novelli L; Ferri R
    Curr Opin Pulm Med; 2010 Nov; 16(6):568-73. PubMed ID: 20814307
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The Kleine-Levin syndrome - effects of treatment with lithium -.
    Poppe M; Friebel D; Reuner U; Todt H; Koch R; Heubner G
    Neuropediatrics; 2003 Jun; 34(3):113-9. PubMed ID: 12910433
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 25.