169 related articles for article (PubMed ID: 29553044)
1. 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]
2. 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]
3. 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]
4. [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]
5. [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]
6. 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]
7. 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]
8. 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]
9. Prader-Willi syndrome in neonates: twenty cases and review of the literature in Southern China.
Wang P; Zhou W; Yuan W; Huang L; Zhao N; Chen X
BMC Pediatr; 2016 Aug; 16():124. PubMed ID: 27506196
[TBL] [Abstract][Full Text] [Related]
10. Perinatal dyskinesia as a presenting feature in Prader Willi syndrome.
McSweeney N; Cowan F; Manzur A; Robb S; Muntoni F
Eur J Paediatr Neurol; 2009 Jul; 13(4):350-5. PubMed ID: 18722147
[TBL] [Abstract][Full Text] [Related]
11. Neonatal hypotonia: don't forget the Prader-Willi syndrome.
Trifirò G; Livieri C; Bosio L; Gargantini L; Corrias A; Pozzan G; Crinò A;
Acta Paediatr; 2003 Sep; 92(9):1085-9. PubMed ID: 14599075
[TBL] [Abstract][Full Text] [Related]
12. 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]
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. 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]
15. [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]
16. Neonatal diagnosis of Prader-Willi syndrome and its implications.
Greenberg F; Elder FF; Ledbetter DH
Am J Med Genet; 1987 Dec; 28(4):845-56. PubMed ID: 3688023
[TBL] [Abstract][Full Text] [Related]
17. Early diagnosis of Prader-Willi syndrome in a newborn.
Chen CJ; Hsu ML; Yuh YS; Cheng SN; Kuo PL; Lee CM
Acta Paediatr Taiwan; 2004; 45(2):108-10. PubMed ID: 15335123
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [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]
20. Clinical and Molecular Characterization of Prader-Willi Syndrome.
Sanjeeva GN; Maganthi M; Kodishala H; Marol RKR; Kulshreshtha PS; Lorenzetto E; Kadandale JS; Hladnik U; Raghupathy P; Bhat M
Indian J Pediatr; 2017 Nov; 84(11):815-821. PubMed ID: 28660389
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]