198 related articles for article (PubMed ID: 24314195)
41. Hypoglycemia in Beckwith-Wiedemann syndrome.
DeBaun MR; King AA; White N
Semin Perinatol; 2000 Apr; 24(2):164-71. PubMed ID: 10805171
[TBL] [Abstract][Full Text] [Related]
42. Diffuse infantile hepatic hemangiomas in a patient with Beckwith-Wiedemann syndrome: A new association?
Macchiaiolo M; Markowich AH; Diociaiuti A; Gonfiantini MV; Buonuomo PS; Rana I; Monti L; El Hachem M; Bartuli A
Am J Med Genet A; 2020 Aug; 182(8):1972-1976. PubMed ID: 32573107
[TBL] [Abstract][Full Text] [Related]
43. Subtotal Pancreatectomy for Congenital Hyperinsulinism: Our Experience and Review of Literature.
Redkar R; Karkera PJ; Krishnan J; Hathiramani V
Indian J Surg; 2015 Dec; 77(Suppl 3):778-82. PubMed ID: 27011456
[TBL] [Abstract][Full Text] [Related]
44. Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinism.
Arya VB; Senniappan S; Demirbilek H; Alam S; Flanagan SE; Ellard S; Hussain K
PLoS One; 2014; 9(5):e98054. PubMed ID: 24840042
[TBL] [Abstract][Full Text] [Related]
45. Gut Microbiome Profile After Pancreatectomy in Infants With Congenital Hyperinsulinism.
Vajravelu ME; Lee JJ; Mitteer L; Zemel BS; Bittinger K; De León DD
Pancreas; 2021 Jan; 50(1):89-92. PubMed ID: 33370028
[TBL] [Abstract][Full Text] [Related]
46. Hypopituitarism in a patient with Beckwith-Wiedemann syndrome due to hypomethylation of KvDMR1.
Baiocchi M; Yousuf FS; Hussain K
Pediatrics; 2014 Apr; 133(4):e1082-6. PubMed ID: 24639276
[TBL] [Abstract][Full Text] [Related]
47. Pancreatic head resection and Roux-en-Y pancreaticojejunostomy for the treatment of the focal form of congenital hyperinsulinism.
Laje P; Stanley CA; Palladino AA; Becker SA; Adzick NS
J Pediatr Surg; 2012 Jan; 47(1):130-5. PubMed ID: 22244405
[TBL] [Abstract][Full Text] [Related]
48. Genomic profiles of a hepatoblastoma from a patient with Beckwith-Wiedemann syndrome with uniparental disomy on chromosome 11p15 and germline mutation of APC and PALB2.
Kim SY; Jung SH; Kim MS; Han MR; Park HC; Jung ES; Lee SH; Lee SH; Chung YJ
Oncotarget; 2017 Nov; 8(54):91950-91957. PubMed ID: 29190888
[TBL] [Abstract][Full Text] [Related]
49. Rare association of Beckwith-Wiedemann syndrome with Hirschsprung's disease in an infant with hypoglycemia.
Shah N; Khadilkar A; Khadilkar V; Lad S
BMJ Case Rep; 2020 Apr; 13(4):. PubMed ID: 32341092
[TBL] [Abstract][Full Text] [Related]
50. The added value of [18F]fluoro-L-DOPA PET in the diagnosis of hyperinsulinism of infancy: a retrospective study involving 49 children.
Ribeiro MJ; Boddaert N; Bellanné-Chantelot C; Bourgeois S; Valayannopoulos V; Delzescaux T; Jaubert F; Nihoul-Fékété C; Brunelle F; De Lonlay P
Eur J Nucl Med Mol Imaging; 2007 Dec; 34(12):2120-8. PubMed ID: 17661030
[TBL] [Abstract][Full Text] [Related]
51. The clinical course of an overgrowth syndrome, from diagnosis in infancy through adulthood: the case of Beckwith-Wiedemann syndrome.
Pappas JG
Curr Probl Pediatr Adolesc Health Care; 2015 Apr; 45(4):112-7. PubMed ID: 25861997
[TBL] [Abstract][Full Text] [Related]
52. Successful subcutaneous glucagon use for persistent hypoglycaemia in congenital hyperinsulinism.
Neylon OM; Moran MM; Pellicano A; Nightingale M; O'Connell MA
J Pediatr Endocrinol Metab; 2013; 26(11-12):1157-61. PubMed ID: 23813352
[TBL] [Abstract][Full Text] [Related]
53. Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.
Slatter RE; Elliott M; Welham K; Carrera M; Schofield PN; Barton DE; Maher ER
J Med Genet; 1994 Oct; 31(10):749-53. PubMed ID: 7837249
[TBL] [Abstract][Full Text] [Related]
54. Mosaic paternal genome-wide uniparental isodisomy with down syndrome.
Darcy D; Atwal PS; Angell C; Gadi I; Wallerstein R
Am J Med Genet A; 2015 Oct; 167A(10):2463-9. PubMed ID: 26219535
[TBL] [Abstract][Full Text] [Related]
55. Renal abnormalities in beckwith-wiedemann syndrome are associated with 11p15.5 uniparental disomy.
Goldman M; Smith A; Shuman C; Caluseriu O; Wei C; Steele L; Ray P; Sadowski P; Squire J; Weksberg R; Rosenblum ND
J Am Soc Nephrol; 2002 Aug; 13(8):2077-84. PubMed ID: 12138139
[TBL] [Abstract][Full Text] [Related]
56. Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia.
Fournet JC; Verkarre V; De Lonlay P; Rahier J; Brunelle F; Robert JJ; Nihoul-Fékété C; Saudubray JM; Junien C
Ann Endocrinol (Paris); 1998; 59(6):485-91. PubMed ID: 10189991
[TBL] [Abstract][Full Text] [Related]
57. Severe presentation of Beckwith-Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15.
Smith AC; Shuman C; Chitayat D; Steele L; Ray PN; Bourgeois J; Weksberg R
Am J Med Genet A; 2007 Dec; 143A(24):3010-5. PubMed ID: 18000906
[TBL] [Abstract][Full Text] [Related]
58. Retrospective analysis of 23 Chinese children with congenital hyperinsulinism undergoing pancreatectomy.
Zhang L; Xu ZD; Liu M; Zeng Q; Li RM; Wang JY; Wang HM; Li L; Qin H; Yan J; Wu YJ; Zhu C; Ni GC; Sang YM
Endokrynol Pol; 2021; 72(5):584-585. PubMed ID: 34292572
[TBL] [Abstract][Full Text] [Related]
59. Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important.
Eggermann T; Brück J; Knopp C; Fekete G; Kratz C; Tasic V; Kurth I; Elbracht M; Eggermann K; Begemann M
J Mol Med (Berl); 2020 Oct; 98(10):1447-1455. PubMed ID: 32839827
[TBL] [Abstract][Full Text] [Related]
60. Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy. A one-decade single-center experience.
Al-Badi MK; Al-Azkawi HS; Al-Yahyaei MS; Mula-Abed WA; Al-Senani AM
Saudi Med J; 2019 Jul; 40(7):669-674. PubMed ID: 31287126
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]