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 *

158 related articles for article (PubMed ID: 26573975)

  • 1. Case report: Dental management of Berardinelli-Seip congenital lipodystrophy.
    Bhujel N; Clark H
    Eur Arch Paediatr Dent; 2016 Apr; 17(2):137-40. PubMed ID: 26573975
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Talon cusps, macrodontia, and aberrant tooth morphology in Berardinelli-Seip syndrome.
    Solanki M; Patil SS; Baweja DK; Noorani H; Pk S
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Jan; 105(1):e41-7. PubMed ID: 18155601
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Severe cardiac phenotype of Berardinelli-Seip congenital lipodystrophy in an infant with homozygous E189X BSCL2 mutation.
    Friguls B; Coroleu W; del Alcazar R; Hilbert P; Van Maldergem L; Pintos-Morell G
    Eur J Med Genet; 2009; 52(1):14-6. PubMed ID: 19041432
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-phenotype correlations of Berardinelli-Seip congenital lipodystrophy and novel candidate genes prediction.
    Ren M; Shi J; Jia J; Guo Y; Ni X; Shi T
    Orphanet J Rare Dis; 2020 Apr; 15(1):108. PubMed ID: 32349771
    [TBL] [Abstract][Full Text] [Related]  

  • 5. AGPAT2 gene mutation in a child with Berardinelli-Seip congenital lipodystrophy syndrome.
    Rostami P; Nakhaeimoghadam M; Bijani FM; Sotoudeh A; Rabbani A; Hilbert P; Rezaei N
    Ann Endocrinol (Paris); 2013 Feb; 74(1):59-61. PubMed ID: 23337016
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case of Berardinelli-Seip syndrome presenting with cirrhosis.
    Wimalaratna H; Nandasiri AS
    J R Coll Physicians Edinb; 2013; 43(4):309-11. PubMed ID: 24350312
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Berardinelli-Seip congenital lipodystrophy: an autosomal recessive disorder with rare association of duodenocolonic polyps.
    Agrawala RK; Choudhury AK; Mohanty BK; Baliarsinha AK
    J Pediatr Endocrinol Metab; 2014 Sep; 27(9-10):989-91. PubMed ID: 24825083
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Berardinelli-Seip Congenital Generalised Lipodystrophy.
    Cheema HA; Malik HS; Waheed N; Mushtaq I; Fayyaz Z; Anjum MN
    J Coll Physicians Surg Pak; 2018 May; 28(5):406-408. PubMed ID: 29690976
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Higher adiponectin levels in patients with Berardinelli-Seip congenital lipodystrophy due to seipin as compared with 1-acylglycerol-3-phosphate-o-acyltransferase-2 deficiency.
    Antuna-Puente B; Boutet E; Vigouroux C; Lascols O; Slama L; Caron-Debarle M; Khallouf E; Lévy-Marchal C; Capeau J; Bastard JP; Magré J
    J Clin Endocrinol Metab; 2010 Mar; 95(3):1463-8. PubMed ID: 20097706
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel mutations of the BSCL2 and AGPAT2 genes in 10 families with Berardinelli-Seip congenital generalized lipodystrophy syndrome.
    Miranda DM; Wajchenberg BL; Calsolari MR; Aguiar MJ; Silva JM; Ribeiro MG; Fonseca C; Amaral D; Boson WL; Resende BA; De Marco L
    Clin Endocrinol (Oxf); 2009 Oct; 71(4):512-7. PubMed ID: 19226263
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The worldwide mutational landscape of Berardinelli-Seip congenital lipodystrophy.
    Craveiro Sarmento AS; Ferreira LC; Lima JG; de Azevedo Medeiros LB; Barbosa Cunha PT; Agnez-Lima LF; Galvão Ururahy MA; de Melo Campos JTA
    Mutat Res Rev Mutat Res; 2019; 781():30-52. PubMed ID: 31416577
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Berardinelli-Seip congenital lipodystrophy in two siblings.
    Rao TS; Chennamsetty K
    Indian Dermatol Online J; 2014 Nov; 5(Suppl 1):S20-2. PubMed ID: 25506557
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Berardinelli-Seip Congenital Lipodystrophy Discovered Following a STEMI Event.
    Beires F; Greenfield H; Brito da Silva J; Gil J; Moreno N
    Eur J Case Rep Intern Med; 2022; 9(12):003658. PubMed ID: 36632537
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Berardinelli Seip Syndrome: A rare case report.
    Ashraf S; Masood S; Naz F; Rashid J
    J Pak Med Assoc; 2022 May; 72(5):969-971. PubMed ID: 35713067
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital Generalized Lipoatrophy (Berardinelli-Seip Syndrome) Type 1: Description of Novel
    Ceccarini G; Magno S; Pelosini C; Ferrari F; Sessa MR; Scabia G; Maffei M; Jéru I; Lascols O; Vigouroux C; Santini F
    Front Endocrinol (Lausanne); 2020; 11():39. PubMed ID: 32117065
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and molecular aspects of Berardinelli-Seip Congenital Lipodystrophy (BSCL).
    Gomes KB; Pardini VC; Fernandes AP
    Clin Chim Acta; 2009 Apr; 402(1-2):1-6. PubMed ID: 19167372
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Early course of Berardinelli-Seip congenital lipodystrophy (BSCL).
    Eltermann T; Menendez-Castro C; Kienzle HP; Wössner R; Thomas W
    Klin Padiatr; 2010 Sep; 222(5):308-9. PubMed ID: 20301053
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Berardinelli-Seip syndrome: highlight of treatment challenge.
    Ferraria N; Pedrosa C; Amaral D; Lopes L
    BMJ Case Rep; 2013 Jan; 2013():. PubMed ID: 23362058
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Two Japanese infants with congenital generalized lipodystrophy due to BSCL2 mutations.
    Nishiyama A; Yagi M; Awano H; Okizuka Y; Maeda T; Yoshida S; Takeshima Y; Matsuo M
    Pediatr Int; 2009 Dec; 51(6):775-9. PubMed ID: 19438831
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.