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)

  • 21. Founder effect of the 669insA mutation in BSCL2 gene causing Berardinelli-Seip congenital lipodystrophy in a cluster from Brazil.
    Gomes KB; Pardini VC; Ferreira AC; Fonseca CG; Fernandes AP
    Ann Hum Genet; 2007 Nov; 71(Pt 6):729-34. PubMed ID: 17535271
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Seipin deficiency alters fatty acid Delta9 desaturation and lipid droplet formation in Berardinelli-Seip congenital lipodystrophy.
    Boutet E; El Mourabit H; Prot M; Nemani M; Khallouf E; Colard O; Maurice M; Durand-Schneider AM; Chrétien Y; Grès S; Wolf C; Saulnier-Blache JS; Capeau J; Magré J
    Biochimie; 2009 Jun; 91(6):796-803. PubMed ID: 19278620
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Further delineation of AGPAT2 and BSCL2 related congenital generalized lipodystrophy in young infants.
    Liu Y; Li D; Ding Y; Kang L; Jin Y; Song J; Li H; Yang Y
    Eur J Med Genet; 2019 Sep; 62(9):103542. PubMed ID: 30266686
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Berardinelli-Seip syndrome and achalasia: a shared pathomechanism?
    van der Pol RJ; Benninga MA; Magré J; Van Maldergem L; Rotteveel J; van der Knaap MS; de Meij TG
    Eur J Pediatr; 2015 Jul; 174(7):975-80. PubMed ID: 25994244
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Congenital generalized lipodystrophy of Berardinelli-Seip type: a rare case.
    Khandpur S; Kumar A; Khadgawat R
    Indian J Dermatol Venereol Leprol; 2011; 77(3):402. PubMed ID: 21508592
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A very rare cause of acute pancreatitis: Berardinelli-Seip congenital lipodystrophy.
    İşlek A; Sayar E; Yılmaz A; Duman Ö; Artan R
    Turk J Gastroenterol; 2014 Dec; 25 Suppl 1():216-9. PubMed ID: 25910311
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Deletion mutation in BSCL2 gene underlies congenital generalized lipodystrophy in a Pakistani family.
    Rahman OU; Khawar N; Khan MA; Ahmed J; Khattak K; Al-Aama JY; Naeem M; Jelani M
    Diagn Pathol; 2013 May; 8():78. PubMed ID: 23659685
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Berardinelli-Seip congenital lipodystrophy.
    Mandal K; Aneja S; Seth A; Khan A
    Indian Pediatr; 2006 May; 43(5):440-5. PubMed ID: 16735770
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Pseudoacromegaly in congenital generalised lipodystrophy (Berardinelli-Seip syndrome).
    Chakraborty PP; Datta S; Mukhopadhyay S; Chowdhury S
    BMJ Case Rep; 2016 Apr; 2016():10.1136/bcr-2016-214493. PubMed ID: 27068725
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Berardinelli-Seip Congenital Lipodystrophy - A Case Report and Review of Literature.
    Munir A; Haider M; Chachar AZK
    J Coll Physicians Surg Pak; 2022 Jun; 32(6):817-819. PubMed ID: 35686420
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A Patient with Berardinelli-Seip Syndrome, Novel
    Oswiecimska J; Dawidziuk M; Gambin T; Ziora K; Marek M; Rzonca S; Guilbride DL; Jhangiani SN; Obuchowicz A; Sikora A; Lupski JR; Wiszniewski W; Gawlinski P
    J Clin Res Pediatr Endocrinol; 2019 Sep; 11(3):319-326. PubMed ID: 30563316
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Berardinelli-Seip lipodystrophy.
    Kobashi Y; Schoenbaum A; Hasserjian RP; Rosenthal DI
    Skeletal Radiol; 2007 Oct; 36(10):999-1003. PubMed ID: 17554536
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Dental and periodontal alterations in Berardinelli-Seip syndrome.
    Lima DL; Montenegro Júnior RM; Fernandes VO; Barros AI; Rêgo DM
    J Int Acad Periodontol; 2007 Apr; 9(2):63-7. PubMed ID: 17506386
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy.
    Kim CA; Delépine M; Boutet E; El Mourabit H; Le Lay S; Meier M; Nemani M; Bridel E; Leite CC; Bertola DR; Semple RK; O'Rahilly S; Dugail I; Capeau J; Lathrop M; Magré J
    J Clin Endocrinol Metab; 2008 Apr; 93(4):1129-34. PubMed ID: 18211975
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Successful long-term use of pioglitazone in Berardinelli-Seip lipodystrophy-associated diabetes.
    Chaves C; Chaves M; Anselmo J; César R
    Endocrinol Diabetes Metab Case Rep; 2021 Apr; 2021():. PubMed ID: 33880995
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Genetic and metabolic description of five patients with Berardinelli-Seip syndrome].
    Barra CB; Savoldelli RD; Manna TD; Kim CA; Magre J; Porta G; Setian N; Damiani D
    Arq Bras Endocrinol Metabol; 2011 Feb; 55(1):54-9. PubMed ID: 21468520
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Early infantile cardiomyopathy and liver disease: a multisystemic disorder caused by congenital lipodystrophy.
    Debray FG; Baguette C; Colinet S; Van Maldergem L; Verellen-Dumouin C
    Mol Genet Metab; 2013 Jun; 109(2):227-9. PubMed ID: 23647707
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Impairment of respiratory muscle strength in Berardinelli-Seip congenital lipodystrophy subjects.
    Dantas de Medeiros JL; Carneiro Bezerra B; Brito de Araújo TA; Craveiro Sarmento AS; de Azevedo Medeiros LB; Peroni Gualdi L; Luna Cruz MDS; Xavier Nobre TT; Gomes Lima J; Araújo de Melo Campos JT
    Respir Res; 2018 Sep; 19(1):173. PubMed ID: 30208912
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome.
    Schrauwen I; Szelinger S; Siniard AL; Kurdoglu A; Corneveaux JJ; Malenica I; Richholt R; Van Camp G; De Both M; Swaminathan S; Turk M; Ramsey K; Craig DW; Narayanan V; Huentelman MJ
    PLoS One; 2015; 10(7):e0131797. PubMed ID: 26176221
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Function of seipin: new insights from Bscl2/seipin knockout mouse models.
    Dollet L; Magré J; Cariou B; Prieur X
    Biochimie; 2014 Jan; 96():166-72. PubMed ID: 23831461
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.