Similar articles for PMID: 32021365

Year	Number of Results
1991	1
1998	1
2001	1
2002	2
2004	1
2005	4
2007	2
2008	2
2009	3
2011	2
2012	2
2013	2
2014	4
2015	10
2016	4
2017	7
2018	7
2019	10
2020	13
2021	10
2024	0

1

Clinical and Molecular Investigation of Familial Multiple Lipomatosis: Variants in the HMGA2 Gene.

Mejía Granados DM, de Baptista MB, Bonadia LC, Bertuzzo CS, Steiner CE. Mejía Granados DM, et al. Clin Cosmet Investig Dermatol. 2020 Jan 7;13:1-10. doi: 10.2147/CCID.S213139. eCollection 2020. Clin Cosmet Investig Dermatol. 2020. PMID: 32021365 Free PMC article.

2

Encephalocraniocutaneous lipomatosis (ECCL) in a patient with history of familial multiple lipomatosis (FML).

Prontera P, Stangoni G, Manes I, Mencarelli A, Donti E. Prontera P, et al. Am J Med Genet A. 2009 Mar;149A(3):543-5. doi: 10.1002/ajmg.a.32692. Am J Med Genet A. 2009. PMID: 19215040 No abstract available.

3

Gastroduodenal Lipomatosis in Familial Multiple Lipomatosis.

Djuric-Stefanovic A, Ebrahimi K, Sisevic J, Saranovic D. Djuric-Stefanovic A, et al. Med Princ Pract. 2017;26(2):189-191. doi: 10.1159/000454714. Epub 2016 Nov 24. Med Princ Pract. 2017. PMID: 27884011 Free PMC article.

4

Expression of HMGA2-LPP and LPP-HMGA2 fusion genes in lipoma: identification of a novel type of LPP-HMGA2 transcript in four cases.

Kubo T, Matsui Y, Naka N, Araki N, Goto T, Yukata K, Endo K, Yasui N, Myoui A, Kawabata H, Yoshikawa H, Ueda T. Kubo T, et al. Anticancer Res. 2009 Jun;29(6):2357-60. Anticancer Res. 2009. PMID: 19528502 Free article.

5

Multiple symmetric and multiple familial lipomatosis.

Lemaitre M, Chevalier B, Jannin A, Bourry J, Espiard S, Vantyghem MC. Lemaitre M, et al. Presse Med. 2021 Nov;50(3):104077. doi: 10.1016/j.lpm.2021.104077. Epub 2021 Oct 21. Presse Med. 2021. PMID: 34687914 Review.

6

Familial multiple lipomatosis: report of a new family.

Gologorsky Y, Gologorsky D, Yarygina AS, Surti U, Zirwas MJ. Gologorsky Y, et al. Cutis. 2007 Mar;79(3):227-32. Cutis. 2007. PMID: 17674589

7

Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.

Riera-Escamilla A, Enguita-Marruedo A, Moreno-Mendoza D, Chianese C, Sleddens-Linkels E, Contini E, Benelli M, Natali A, Colpi GM, Ruiz-Castañé E, Maggi M, Baarends WM, Krausz C. Riera-Escamilla A, et al. Hum Reprod. 2019 Jun 4;34(6):978-988. doi: 10.1093/humrep/dez042. Hum Reprod. 2019. PMID: 31125047

8

Syndromic lipomatosis of the head and neck: a review of the literature.

Tadisina KK, Mlynek KS, Hwang LK, Riazi H, Papay FA, Zins JE. Tadisina KK, et al. Aesthetic Plast Surg. 2015 Jun;39(3):440-8. doi: 10.1007/s00266-015-0478-8. Epub 2015 Apr 10. Aesthetic Plast Surg. 2015. PMID: 25860506 Review.

9

Next-generation sequencing for genetic testing of familial colorectal cancer syndromes.

Simbolo M, Mafficini A, Agostini M, Pedrazzani C, Bedin C, Urso ED, Nitti D, Turri G, Scardoni M, Fassan M, Scarpa A. Simbolo M, et al. Hered Cancer Clin Pract. 2015 Aug 21;13(1):18. doi: 10.1186/s13053-015-0039-9. eCollection 2015. Hered Cancer Clin Pract. 2015. PMID: 26300997 Free PMC article.

10

Next-generation sequencing to solve complex inherited retinal dystrophy: A case series of multiple genes contributing to disease in extended families.

Jones KD, Wheaton DK, Bowne SJ, Sullivan LS, Birch DG, Chen R, Daiger SP. Jones KD, et al. Mol Vis. 2017 Jul 20;23:470-481. eCollection 2017. Mol Vis. 2017. PMID: 28761320 Free PMC article.

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