165 related articles for article (PubMed ID: 34110109)
21. Cerebroretinal microangiopathy with calcifications and cysts (CRMCC) or "Coats Plus": when peripheral retinal vasculature signals neurologic disease.
Mansukhani S; Ho ML; Gavrilova RH; Mohney BG; Quiram PA; Brodsky MC
J AAPOS; 2017 Oct; 21(5):420-422. PubMed ID: 28864049
[TBL] [Abstract][Full Text] [Related]
22. [Coats Plus: Coats disease with systemic features].
Troumani Y; Ackermann F; Cohen S; Touhami S; Nasser G; Denier C; Labetoulle M; Rousseau A
J Fr Ophtalmol; 2016 Sep; 39(7):e167-70. PubMed ID: 27546161
[No Abstract] [Full Text] [Related]
23. Identification of novel SNORD118 mutations in seven patients with leukoencephalopathy with brain calcifications and cysts.
Iwama K; Mizuguchi T; Takanashi JI; Shibayama H; Shichiji M; Ito S; Oguni H; Yamamoto T; Sekine A; Nagamine S; Ikeda Y; Nishida H; Kumada S; Yoshida T; Awaya T; Tanaka R; Chikuchi R; Niwa H; Oka YI; Miyatake S; Nakashima M; Takata A; Miyake N; Ito S; Saitsu H; Matsumoto N
Clin Genet; 2017 Aug; 92(2):180-187. PubMed ID: 28177126
[TBL] [Abstract][Full Text] [Related]
24. Gastrointestinal Hemorrhage: A Manifestation of the Telomere Biology Disorders.
Himes RW; Chiou EH; Queliza K; Shouval DS; Somech R; Agarwal S; Jajoo K; Ziegler DS; Kratz CP; Huang J; Lucas TL; Myers KC; Nelson AS; DiNardo CD; Alter BP; Giri N; Khincha PP; McReynolds LJ; Dufour C; Pierri F; Goldman FD; Sherif Y; Savage SA; Miloh T; Bertuch AA
J Pediatr; 2021 Mar; 230():55-61.e4. PubMed ID: 32971146
[TBL] [Abstract][Full Text] [Related]
25. Retinopathy and bone marrow failure revealing Coats plus syndrome.
Painho T; Conceição C; Kjöllerström P; Batalha S
BMJ Case Rep; 2018 Mar; 2018():. PubMed ID: 29523622
[No Abstract] [Full Text] [Related]
26. Progressive cerebroretinal microangiopathy with calcifications and cysts syndrome: an unusual cause of complex partial seizure.
Dusak A; Seferoğlu M; Hakyemez B; Bora I; Parlak M
Psychiatry Clin Neurosci; 2012 Aug; 66(5):460. PubMed ID: 22834668
[No Abstract] [Full Text] [Related]
27. Coats plus syndrome: a rare cause of severe gastrointestinal tract bleeding in children - a case report.
Bozkurt S; Usta AM; Urganci N; Kalay NG; Kose G; Ozmen E
BMC Pediatr; 2022 Mar; 22(1):119. PubMed ID: 35260125
[TBL] [Abstract][Full Text] [Related]
28. [Neuroimaging findings in cerebroretinal microangiopathy with calcifications and cysts].
Herrera DA; Vargas SA; Montoya C
Biomedica; 2014; 34(2):166-70. PubMed ID: 24967922
[TBL] [Abstract][Full Text] [Related]
29. Coats plus in prematurity.
López-Cañizares A; Fernandez MP; Al-Khersan H; Carletti P; Arroyo MS; Fernandez-Ruiz MC; Berrocal AM
Ophthalmic Genet; 2022 Aug; 43(4):543-549. PubMed ID: 35416114
[TBL] [Abstract][Full Text] [Related]
30. A case of late-onset leukoencephalopathy, calcifications, and cysts presenting with intracerebral hemorrhage resembling a neoplasm.
Banks GP; Weiss SA; Pisapia D; Willey JZ
Cerebrovasc Dis; 2013; 35(4):396-7. PubMed ID: 23635489
[No Abstract] [Full Text] [Related]
31. Coats plus syndrome (cerebroretinal microangiopathy with calcifications and cysts-1): A case report.
Morgado F; Batista M; Moreno A; Coutinho I
Pediatr Dermatol; 2021 Jan; 38(1):191-193. PubMed ID: 33010065
[TBL] [Abstract][Full Text] [Related]
32. CTC1-STN1 coordinates G- and C-strand synthesis to regulate telomere length.
Gu P; Jia S; Takasugi T; Smith E; Nandakumar J; Hendrickson E; Chang S
Aging Cell; 2018 Aug; 17(4):e12783. PubMed ID: 29774655
[TBL] [Abstract][Full Text] [Related]
33. Coats-plus syndrome: when imaging leads to genetic diagnosis.
Maia C; Batista M; Palavra F; Pinto J
BMJ Case Rep; 2022 May; 15(5):. PubMed ID: 35580952
[No Abstract] [Full Text] [Related]
34. Mutations in CTC1, encoding the CTS telomere maintenance complex component 1, cause cerebroretinal microangiopathy with calcifications and cysts.
Polvi A; Linnankivi T; Kivelä T; Herva R; Keating JP; Mäkitie O; Pareyson D; Vainionpää L; Lahtinen J; Hovatta I; Pihko H; Lehesjoki AE
Am J Hum Genet; 2012 Mar; 90(3):540-9. PubMed ID: 22387016
[TBL] [Abstract][Full Text] [Related]
35. Coats Plus syndrome: a diagnostic and therapeutic challenge in pediatric gastrointestinal hemorrhage.
Hoşnut FÖ; Şahin G; Akçaboy M
Turk J Pediatr; 2022; 64(1):166-170. PubMed ID: 35286046
[TBL] [Abstract][Full Text] [Related]
36. Mutations in the telomere capping complex in bone marrow failure and related syndromes.
Walne AJ; Bhagat T; Kirwan M; Gitiaux C; Desguerre I; Leonard N; Nogales E; Vulliamy T; Dokal IS
Haematologica; 2013 Mar; 98(3):334-8. PubMed ID: 22899577
[TBL] [Abstract][Full Text] [Related]
37. Human TEN1 maintains telomere integrity and functions in genome-wide replication restart.
Kasbek C; Wang F; Price CM
J Biol Chem; 2013 Oct; 288(42):30139-30150. PubMed ID: 24025336
[TBL] [Abstract][Full Text] [Related]
38. Leukoencephalopathy with calcifications and cysts: a purely neurological disorder distinct from coats plus.
Livingston JH; Mayer J; Jenkinson E; Kasher P; Stivaros S; Berger A; Cordelli DM; Ferreira P; Jefferson R; Kutschke G; Lundberg S; Ounap K; Prabhakar P; Soh C; Stewart H; Stone J; van der Knaap MS; van Esch H; van Mol C; Wakeling E; Whitney A; Rice GI; Crow YJ
Neuropediatrics; 2014 Jun; 45(3):175-82. PubMed ID: 24407470
[TBL] [Abstract][Full Text] [Related]
39. Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature review.
Osman O; Labrune P; Reiner P; Sarov M; Nasser G; Riant F; Tournier-Lasserve E; Chabriat H; Denier C
Rev Neurol (Paris); 2020 Mar; 176(3):170-179. PubMed ID: 31521395
[TBL] [Abstract][Full Text] [Related]
40. CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures.
Sargolzaeiaval F; Zhang J; Schleit J; Lessel D; Kubisch C; Precioso DR; Sillence D; Hisama FM; Dorschner M; Martin GM; Oshima J
Mol Genet Genomic Med; 2018 Nov; 6(6):1148-1156. PubMed ID: 30393977
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]