BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

235 related articles for article (PubMed ID: 38396741)

  • 1. The Pivotal Role of Oxytocin's Mechanism of Thermoregulation in Prader-Willi Syndrome, Schaaf-Yang Syndrome, and Autism Spectrum Disorder.
    Camerino C
    Int J Mol Sci; 2024 Feb; 25(4):. PubMed ID: 38396741
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Oxytocin's Regulation of Thermogenesis May Be the Link to Prader-Willi Syndrome.
    Camerino C
    Curr Issues Mol Biol; 2023 Jun; 45(6):4923-4935. PubMed ID: 37367062
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hormonal, metabolic and skeletal phenotype of Schaaf-Yang syndrome: a comparison to Prader-Willi syndrome.
    McCarthy JM; McCann-Crosby BM; Rech ME; Yin J; Chen CA; Ali MA; Nguyen HN; Miller JL; Schaaf CP
    J Med Genet; 2018 May; 55(5):307-315. PubMed ID: 29496979
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Schaaf-Yang Syndrome: Clinical Phenotype and Effects of 4 years of Growth Hormone Treatment.
    Juriaans AF; Kerkhof GF; Garrelfs M; Trueba-Timmermans D; Hokken-Koelega ACS
    Horm Res Paediatr; 2024; 97(2):148-156. PubMed ID: 37343528
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prader-Willi Syndrome and Schaaf-Yang Syndrome: Neurodevelopmental Diseases Intersecting at the
    Fountain MD; Schaaf CP
    Diseases; 2016 Jan; 4(1):. PubMed ID: 28933382
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Autism spectrum disorder in Prader-Willi syndrome: A systematic review.
    Bennett JA; Germani T; Haqq AM; Zwaigenbaum L
    Am J Med Genet A; 2015 Dec; 167A(12):2936-44. PubMed ID: 26331980
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Spectrum of the Prader-Willi-like Pheno- and Genotype: A Review of the Literature.
    Juriaans AF; Kerkhof GF; Hokken-Koelega ACS
    Endocr Rev; 2022 Jan; 43(1):1-18. PubMed ID: 34460908
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Oxytocin-based therapies for treatment of Prader-Willi and Schaaf-Yang syndromes: evidence, disappointments, and future research strategies.
    Althammer F; Muscatelli F; Grinevich V; Schaaf CP
    Transl Psychiatry; 2022 Aug; 12(1):318. PubMed ID: 35941105
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Early Social Cognitive Ability in Preschoolers with Prader-Willi Syndrome and Autism Spectrum Disorder.
    Dimitropoulos A; Zyga O; Russ SW
    J Autism Dev Disord; 2019 Nov; 49(11):4441-4454. PubMed ID: 31388797
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families.
    Fountain MD; Aten E; Cho MT; Juusola J; Walkiewicz MA; Ray JW; Xia F; Yang Y; Graham BH; Bacino CA; Potocki L; van Haeringen A; Ruivenkamp CA; Mancias P; Northrup H; Kukolich MK; Weiss MM; van Ravenswaaij-Arts CM; Mathijssen IB; Levesque S; Meeks N; Rosenfeld JA; Lemke D; Hamosh A; Lewis SK; Race S; Stewart LL; Hay B; Lewis AM; Guerreiro RL; Bras JT; Martins MP; Derksen-Lubsen G; Peeters E; Stumpel C; Stegmann S; Bok LA; Santen GW; Schaaf CP
    Genet Med; 2017 Jan; 19(1):45-52. PubMed ID: 27195816
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
    Angulo MA; Butler MG; Cataletto ME
    J Endocrinol Invest; 2015 Dec; 38(12):1249-63. PubMed ID: 26062517
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neurocognitive and Neurobehavioral Phenotype of Youth with Schaaf-Yang Syndrome.
    Thomason MM; McCarthy J; Goin-Kochel RP; Dowell LR; Schaaf CP; Berry LN
    J Autism Dev Disord; 2020 Jul; 50(7):2491-2500. PubMed ID: 30343463
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital ichthyosis in Prader-Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD.
    Muthusamy K; Macke EL; Klee EW; Tebben PJ; Hand JL; Hasadsri L; Marcou CA; Schimmenti LA
    Am J Med Genet A; 2020 Oct; 182(10):2442-2449. PubMed ID: 32815268
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy.
    Negishi Y; Ieda D; Hori I; Nozaki Y; Yamagata T; Komaki H; Tohyama J; Nagasaki K; Tada H; Saitoh S
    Orphanet J Rare Dis; 2019 Dec; 14(1):277. PubMed ID: 31791363
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A girl with incomplete Prader-Willi syndrome and negative MS-PCR, found to have mosaic maternal UPD-15 at SNP array.
    Morandi A; Bonnefond A; Lobbens S; Carotenuto M; Del Giudice EM; Froguel P; Maffeis C
    Am J Med Genet A; 2015 Nov; 167A(11):2720-6. PubMed ID: 26109092
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review.
    Hartin SN; Hossain WA; Weisensel N; Butler MG
    Am J Med Genet A; 2018 Apr; 176(4):886-895. PubMed ID: 29437285
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A study of voice and non-voice processing in Prader-Willi syndrome.
    Strenilkov K; Debladis J; Salles J; Valette M; Mantoulan C; Thuilleaux D; Laurier V; Molinas C; Barone P; Tauber M
    Orphanet J Rare Dis; 2020 Jan; 15(1):22. PubMed ID: 31959191
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches.
    Butler MG; Manzardo AM; Forster JL
    Curr Pediatr Rev; 2016; 12(2):136-66. PubMed ID: 26592417
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Investigating Autism-Related Symptoms in Children with Prader-Willi Syndrome: A Case Study.
    Bennett JA; Hodgetts S; Mackenzie ML; Haqq AM; Zwaigenbaum L
    Int J Mol Sci; 2017 Feb; 18(3):. PubMed ID: 28264487
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.