BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

242 related articles for article (PubMed ID: 32922110)

  • 41. Changing rates of genetic subtypes of Prader-Willi syndrome in the UK.
    Whittington JE; Butler JV; Holland AJ
    Eur J Hum Genet; 2007 Jan; 15(1):127-30. PubMed ID: 16957680
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Prader- Willi syndrome: An uptodate on endocrine and metabolic complications.
    Muscogiuri G; Formoso G; Pugliese G; Ruggeri RM; Scarano E; Colao A;
    Rev Endocr Metab Disord; 2019 Jun; 20(2):239-250. PubMed ID: 31065942
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Prader-Willi syndrome: From genetics to behaviour, with special focus on appetite treatments.
    Griggs JL; Sinnayah P; Mathai ML
    Neurosci Biobehav Rev; 2015 Dec; 59():155-72. PubMed ID: 26475993
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Hyperphagia in Prader-Willi syndrome with obesity: From development to pharmacological treatment.
    Rahman QFA; Jufri NF; Hamid A
    Intractable Rare Dis Res; 2023 Feb; 12(1):5-12. PubMed ID: 36873672
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
    Goldstone AP
    Trends Endocrinol Metab; 2004; 15(1):12-20. PubMed ID: 14693421
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Neonatal presentation of Prader-Willi syndrome: A report of five cases].
    Richard-De Ceaurriz B; Leymarie C; Godefroy A; Collignon P; Sigaudy S; Truc P
    Arch Pediatr; 2017 Nov; 24(11):1115-1120. PubMed ID: 28967604
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome.
    Cheon CK
    Ann Pediatr Endocrinol Metab; 2016 Sep; 21(3):126-135. PubMed ID: 27777904
    [TBL] [Abstract][Full Text] [Related]  

  • 48. From Prader-Willi syndrome to psychosis: translating parent-of-origin effects into schizophrenia research.
    Krefft M; Frydecka D; Adamowski T; Misiak B
    Epigenomics; 2014; 6(6):677-88. PubMed ID: 25531260
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Prader-Willi syndrome and genomic imprinting].
    Wang W; Wang DF; Cui YF; Ni JH; Dong ZY; Fu MF; Fu HM; Lu GQ; Chen FS
    Zhonghua Er Ke Za Zhi; 2003 Jun; 41(6):453-6. PubMed ID: 14749005
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader-Willi syndrome: an ERP study.
    Stauder JE; Boer H; Gerits RH; Tummers A; Whittington J; Curfs LM
    Clin Neurophysiol; 2005 Jun; 116(6):1464-70. PubMed ID: 15978509
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. Early Detection and Management of Prader-Willi Syndrome in Egyptian Patients.
    El-Bassyouni HT; Hassan N; Mahfouz I; Abd-Elnaby AE; Mostafa MI; Tosson AMS
    J Pediatr Genet; 2019 Dec; 8(4):179-186. PubMed ID: 31687254
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis.
    Buiting K; Dittrich B; Gross S; Lich C; Färber C; Buchholz T; Smith E; Reis A; Bürger J; Nöthen MM; Barth-Witte U; Janssen B; Abeliovich D; Lerer I; van den Ouweland AM; Halley DJ; Schrander-Stumpel C; Smeets H; Meinecke P; Malcolm S; Gardner A; Lalande M; Nicholls RD; Friend K; Schulze A; Matthijs G; Kokkonen H; Hilbert P; Van Maldergem L; Glover G; Carbonell P; Willems P; Gillessen-Kaesbach G; Horsthemke B
    Am J Hum Genet; 1998 Jul; 63(1):170-80. PubMed ID: 9634532
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.
    Driscoll DJ; Waters MF; Williams CA; Zori RT; Glenn CC; Avidano KM; Nicholls RD
    Genomics; 1992 Aug; 13(4):917-24. PubMed ID: 1505981
    [TBL] [Abstract][Full Text] [Related]  

  • 55. The genetic basis for Prader-Willi syndrome: the importance of imprinted genes.
    Brøndum-Nielsen K
    Acta Paediatr Suppl; 1997 Nov; 423():55-7. PubMed ID: 9401540
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons.
    Langouët M; Glatt-Deeley HR; Chung MS; Dupont-Thibert CM; Mathieux E; Banda EC; Stoddard CE; Crandall L; Lalande M
    Hum Mol Genet; 2018 Feb; 27(3):505-515. PubMed ID: 29228278
    [TBL] [Abstract][Full Text] [Related]  

  • 57. First Case Report of Prader-Willi-Like Syndrome in Colombia.
    Candelo E; Feinstein MM; Ramirez-Montaño D; Gomez JF; Pachajoa H
    Front Genet; 2018; 9():98. PubMed ID: 29619043
    [No Abstract]   [Full Text] [Related]  

  • 58. Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.
    Milner KM; Craig EE; Thompson RJ; Veltman MW; Thomas NS; Roberts S; Bellamy M; Curran SR; Sporikou CM; Bolton PF
    J Child Psychol Psychiatry; 2005 Oct; 46(10):1089-96. PubMed ID: 16178933
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Diagnostic and prognostic problems with the Prader-Willi syndrome.
    Kopel J
    Proc (Bayl Univ Med Cent); 2019 Jan; 32(1):167-168. PubMed ID: 30956621
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A genetic condition that spans both extremes of the nutritional spectrum.
    Johnson LM
    Pract Lab Med; 2024 May; 40():e00405. PubMed ID: 38953015
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.