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 *

125 related articles for article (PubMed ID: 36975754)

  • 1. Perinatal and neonatal characteristics of Prader-Willi syndrome in Japan.
    Oto Y; Murakami N; Imatani K; Inoue T; Itabashi H; Shiraishi M; Nitta A; Matsubara K; Kobayashi S; Ihara H; Nagai T; Matsubara T
    Pediatr Int; 2023; 65(1):e15540. PubMed ID: 36975754
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Perinatal features of Prader-Willi syndrome: a Chinese cohort of 134 patients.
    Yang L; Zhou Q; Ma B; Mao S; Dai Y; Zhu M; Zou C
    Orphanet J Rare Dis; 2020 Jan; 15(1):24. PubMed ID: 31964399
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Analysis of the clinical perinatal characteristics of 226 patients with Prader-Willi syndrome in China].
    Zhou Y; Ma MS; Li GY; Zhang ZJ; Ding J; Xu YW; Qiu ZQ; Song HM
    Zhonghua Er Ke Za Zhi; 2021 Jun; 59(6):466-470. PubMed ID: 34102819
    [No Abstract]   [Full Text] [Related]  

  • 4. Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life.
    Çizmecioğlu FM; Jones JH; Paterson WF; Kherra S; Kourime M; McGowan R; Shaikh MG; Donaldson M
    J Clin Res Pediatr Endocrinol; 2018 Jul; 10(3):264-273. PubMed ID: 29553044
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multicentre study of maternal and neonatal outcomes in individuals with Prader-Willi syndrome.
    Singh P; Mahmoud R; Gold JA; Miller JL; Roof E; Tamura R; Dykens E; Butler MG; Driscoll DJ; Kimonis V
    J Med Genet; 2018 Sep; 55(9):594-598. PubMed ID: 29776967
    [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. [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]  

  • 8. Comparison of perinatal factors in deletion versus uniparental disomy in Prader-Willi syndrome.
    Gold JA; Mahmoud R; Cassidy SB; Kimonis V
    Am J Med Genet A; 2018 May; 176(5):1161-1165. PubMed ID: 29681103
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cardiac rhabdomyoma as a possible new prenatal sonographic feature of Prader-Willi syndrome.
    Traisrisilp K; Sirikunalai P; Sirilert S; Chareonsirisuthigul T; Tongsong T
    J Obstet Gynaecol Res; 2022 Jan; 48(1):239-243. PubMed ID: 34655138
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Clinical screening and genetic diagnosis for Prader-Willi syndrome].
    Dong GQ; Su YY; Qiu XY; Lu XY; Li JX; Huang M; Luo XP
    Zhongguo Dang Dai Er Ke Za Zhi; 2020 Sep; 22(9):1001-1006. PubMed ID: 32933634
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prevalence of Prader-Willi syndrome among infants with hypotonia.
    Tuysuz B; Kartal N; Erener-Ercan T; Guclu-Geyik F; Vural M; Perk Y; Erçal D; Erginel-Unaltuna N
    J Pediatr; 2014 May; 164(5):1064-7. PubMed ID: 24582009
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome.
    Bar C; Diene G; Molinas C; Bieth E; Casper C; Tauber M
    Orphanet J Rare Dis; 2017 Jun; 12(1):118. PubMed ID: 28659150
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Relationship between phenotype and genotype of 102 Chinese newborns with Prader-Willi syndrome.
    Ge MM; Gao YY; Wu BB; Yan K; Qin Q; Wang H; Zhou W; Yang L
    Mol Biol Rep; 2019 Oct; 46(5):4717-4724. PubMed ID: 31270759
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical evidence of intrauterine disturbance in Prader-Willi syndrome, a genetically imprinted neurodevelopmental disorder.
    Dudley O; Muscatelli F
    Early Hum Dev; 2007 Jul; 83(7):471-8. PubMed ID: 17055193
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prader-Willi syndrome in Taiwan.
    Lin HY; Lin SP; Yen JL; Lee YJ; Huang CY; Hung HY; Hsu CH; Kao HA; Chang JH; Chiu NC; Ho CS; Chao MC; Niu DM; Tsai LP; Kuo PL
    Pediatr Int; 2007 Jun; 49(3):375-9. PubMed ID: 17532839
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Maternal uniparental disomy 14; differential diagnosis with Prader-Willi syndrome].
    Tamminga S; Stalman SE; Kamp GA; Hendriks YM; Knegt AC; Elting MW
    Ned Tijdschr Geneeskd; 2015; 159():A8240. PubMed ID: 25898865
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Distal arthrogryposis and neonatal hypotonia: an unusual presentation of Prader-Willi syndrome (PWS).
    Denizot S; Boscher C; Le Vaillant C; Rozé JC; Gras Le Guen C
    J Perinatol; 2004 Nov; 24(11):733-4. PubMed ID: 15510104
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Prenatal and Neonatal Characteristics of Children with Prader-Willi Syndrome.
    Grootjen LN; Uyl NEM; van Beijsterveldt IALP; Damen L; Kerkhof GF; Hokken-Koelega ACS
    J Clin Med; 2022 Jan; 11(3):. PubMed ID: 35160130
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.