160 related articles for article (PubMed ID: 21327337)
1. Fanconi-Bickel syndrome.
Mohandas Nair K ; Sakamoto O; Jagadeesh S; Nampoothiri S
Indian J Pediatr; 2012 Jan; 79(1):112-4. PubMed ID: 21327337
[TBL] [Abstract][Full Text] [Related]
2. Fanconi-Bickel syndrome in a 3-year-old Indian boy with a novel mutation in the GLUT2 gene.
Gopalakrishnan A; Kumar M; Krishnamurthy S; Sakamoto O; Srinivasan S
Clin Exp Nephrol; 2011 Oct; 15(5):745-748. PubMed ID: 21625891
[TBL] [Abstract][Full Text] [Related]
3. Fanconi-Bickel syndrome - mutation in SLC2A2 gene.
Kehar M; Bijarnia S; Ellard S; Houghton J; Saxena R; Verma IC; Wadhwa N
Indian J Pediatr; 2014 Nov; 81(11):1237-9. PubMed ID: 24912437
[TBL] [Abstract][Full Text] [Related]
4. Fanconi- Bickel Syndrome: mutation in an Indian patient.
Ekbote AV; Mandal K; Agarwal I; Sinha R; Danda S
Indian J Pediatr; 2012 Jun; 79(6):810-2. PubMed ID: 21972075
[TBL] [Abstract][Full Text] [Related]
5. Fanconi Bickel Syndrome with Hypercalciuria due to GLUT 2 Mutation.
Shah R; Rao S; Parikh R; Sophia T; Khalid H
Indian Pediatr; 2016 Sep; 53(9):829-830. PubMed ID: 27771652
[TBL] [Abstract][Full Text] [Related]
6. Segregation of a novel homozygous 6 nucleotide deletion in GLUT2 gene in a Fanconi-Bickel syndrome family.
Abbasi F; Azizi F; Javaheri M; Mosallanejad A; Ebrahim-Habibi A; Ghafouri-Fard S
Gene; 2015 Feb; 557(1):103-5. PubMed ID: 25523092
[TBL] [Abstract][Full Text] [Related]
7. Transient neonatal diabetes as a presentation of Fanconi- Bickel Syndrome.
Setoodeh A; Rabbani A
Acta Med Iran; 2012; 50(12):836-8. PubMed ID: 23456528
[TBL] [Abstract][Full Text] [Related]
8. Fanconi-Bickel syndrome and autosomal recessive proximal tubulopathy with hypercalciuria (ARPTH) are allelic variants caused by GLUT2 mutations.
Mannstadt M; Magen D; Segawa H; Stanley T; Sharma A; Sasaki S; Bergwitz C; Mounien L; Boepple P; Thorens B; Zelikovic I; Jüppner H
J Clin Endocrinol Metab; 2012 Oct; 97(10):E1978-86. PubMed ID: 22865906
[TBL] [Abstract][Full Text] [Related]
9. Fanconi-Bickel syndrome.
Karande S; Kumbhare N; Kulkarni M
Indian Pediatr; 2007 Mar; 44(3):223-5. PubMed ID: 17413201
[TBL] [Abstract][Full Text] [Related]
10. Fanconi-Bickel Syndrome: Another Novel Mutation in SLC2A2.
Amita M; Srivastava P; Mandal K; De S; Phadke SR
Indian J Pediatr; 2017 Mar; 84(3):236-237. PubMed ID: 27738794
[No Abstract] [Full Text] [Related]
11. Fanconi-Bickel syndrome in three Turkish patients with different homozygous mutations.
Saltik-Temizel IN; Coşkun T; Yüce A; Koçak N
Turk J Pediatr; 2005; 47(2):167-9. PubMed ID: 16052858
[TBL] [Abstract][Full Text] [Related]
12. Genetic testing of two Pakistani patients affected with rare autosomal recessive Fanconi-Bickel syndrome and identification of a novel SLC2A2 splice site variant.
Batool H; Zubaida B; Hashmi MA; Naeem M
J Pediatr Endocrinol Metab; 2019 Nov; 32(11):1229-1233. PubMed ID: 31473689
[TBL] [Abstract][Full Text] [Related]
13. A novel mutation of the GLUT2 gene in a Turkish patient with Fanconi-Bickel syndrome.
Simşek E; Savaş-Erdeve S; Sakamoto O; Doğanci T; Dallar Y
Turk J Pediatr; 2009; 51(2):166-8. PubMed ID: 19480329
[TBL] [Abstract][Full Text] [Related]
14. Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi-Bickel syndrome: revisited gene atlas for renumbering.
Al-Haggar M; Sakamoto O; Shaltout A; Al-Hawari A; Wahba Y; Abdel-Hadi D
Clin Exp Nephrol; 2012 Aug; 16(4):604-10. PubMed ID: 22350464
[TBL] [Abstract][Full Text] [Related]
15. Heterozygous recurrent HNF4A variant p.Arg85Trp causes Fanconi renotubular syndrome 4 with maturity onset diabetes of the young, an autosomal dominant phenocopy of Fanconi Bickel syndrome with colobomas.
Sheppard SE; Barrett B; Muraresku C; McKnight H; De Leon DD; Lord K; Ganetzky R
Am J Med Genet A; 2021 Feb; 185(2):566-570. PubMed ID: 33251707
[TBL] [Abstract][Full Text] [Related]
16. Fanconi-Bickel syndrome: GLUT2 mutations associated with a mild phenotype.
Grünert SC; Schwab KO; Pohl M; Sass JO; Santer R
Mol Genet Metab; 2012 Mar; 105(3):433-7. PubMed ID: 22214819
[TBL] [Abstract][Full Text] [Related]
17. [SLC2A2 gene analysis in three Chinese children with Fanconi-Bickel syndrome].
Wang W; Wei M; Song HM; Qiu ZQ; Zhang LJ; Li Z; Tang XY
Zhongguo Dang Dai Er Ke Za Zhi; 2015 Apr; 17(4):362-6. PubMed ID: 25919556
[TBL] [Abstract][Full Text] [Related]
18. Nocturnal enteral nutrition is therapeutic for growth failure in Fanconi-Bickel syndrome.
Pennisi A; Maranda B; Benoist JF; Baudouin V; Rigal O; Pichard S; Santer R; Romana Lepri F; Novelli A; Ogier de Baulny H; Dionisi-Vici C; Schiff M
J Inherit Metab Dis; 2020 May; 43(3):540-548. PubMed ID: 31816104
[TBL] [Abstract][Full Text] [Related]
19. An Indian girl with Fanconi-Bickel syndrome without SLC2A2 gene mutation.
Dayal D; Dekate P; Sharda S; Das A; Attri S
J Pediatr Genet; 2013 Jun; 2(2):109-12. PubMed ID: 27625848
[TBL] [Abstract][Full Text] [Related]
20. Two cases of Fanconi-Bickel syndrome: first report from China with novel mutations of SLC2A2 gene.
Su Z; Du ML; Chen HS; Chen QL; Yu CS; Mal HM
J Pediatr Endocrinol Metab; 2011; 24(9-10):749-53. PubMed ID: 22145468
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
