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Best matches for loose anagen syndrome:

Moyamoya syndrome in a patient with Noonan-like syndrome with loose anagen hair. Choi JH et al. Pediatr Neurol. (2015)

Loose anagen hair syndrome in black-haired Indian children. Dey V et al. Pediatr Dermatol. (2013)

A case of loose anagen syndrome in an African American girl. Agi C et al. Pediatr Dermatol. (2015)

Search results

Items: 1 to 20 of 103

1.

Noonan syndrome with loose anagen hair associated with trichorrhexis nodosa and trichoptilosis.

Kane J, Berrebi K, McLean R, Petkiewicz S, Hay B, Martin M, Wiss K.

Clin Case Rep. 2017 Jun 1;5(7):1152-1154. doi: 10.1002/ccr3.1011. eCollection 2017 Jul.

2.

Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp.

Bertola D, Buscarilli M, Stabley DL, Baker L, Doyle D, Bartholomew DW, Sol-Church K, Gripp KW.

Am J Med Genet A. 2017 May;173(5):1309-1318. doi: 10.1002/ajmg.a.38178. Epub 2017 Apr 3.

PMID:
28371260
3.

The recurrent PPP1CB mutation p.Pro49Arg in an additional Noonan-like syndrome individual: Broadening the clinical phenotype.

Bertola D, Yamamoto G, Buscarilli M, Jorge A, Passos-Bueno MR, Kim C.

Am J Med Genet A. 2017 Mar;173(3):824-828. doi: 10.1002/ajmg.a.38070. Review.

PMID:
28211982
4.

Noonan syndrome - a new survey.

Tafazoli A, Eshraghi P, Koleti ZK, Abbaszadegan M.

Arch Med Sci. 2017 Feb 1;13(1):215-222. doi: 10.5114/aoms.2017.64720. Epub 2016 Dec 19.

5.

Hair pull test: Evidence-based update and revision of guidelines.

McDonald KA, Shelley AJ, Colantonio S, Beecker J.

J Am Acad Dermatol. 2017 Mar;76(3):472-477. doi: 10.1016/j.jaad.2016.10.002. Epub 2016 Dec 20.

PMID:
28010890
6.

Further evidence that variants in PPP1CB cause a rasopathy similar to Noonan syndrome with loose anagen hair.

Zambrano RM, Marble M, Chalew SA, Lilje C, Vargas A, Lacassie Y.

Am J Med Genet A. 2017 Feb;173(2):565-567. doi: 10.1002/ajmg.a.38056. Epub 2016 Nov 21. No abstract available.

PMID:
27868344
7.

Trichotillomania: Bizzare Patern of Hair Loss at 11-Year-old Girl.

Zímová J, Zímová P.

Acta Dermatovenerol Croat. 2016 Jun;24(2):150-3.

PMID:
27477178
8.

SHOC2 subcellular shuttling requires the KEKE motif-rich region and N-terminal leucine-rich repeat domain and impacts on ERK signalling.

Motta M, Chillemi G, Fodale V, Cecchetti S, Coppola S, Stipo S, Cordeddu V, Macioce P, Gelb BD, Tartaglia M.

Hum Mol Genet. 2016 Sep 1;25(17):3824-3835. doi: 10.1093/hmg/ddw229. Epub 2016 Jul 27.

PMID:
27466182
9.

Loose Anagen Syndrome: A Retrospective Chart Review of 37 Cases.

Swink SM, Castelo-Soccio L.

Pediatr Dermatol. 2016 Sep;33(5):507-10. doi: 10.1111/pde.12912. Epub 2016 Jul 19.

PMID:
27436070
10.

A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair.

Gripp KW, Aldinger KA, Bennett JT, Baker L, Tusi J, Powell-Hamilton N, Stabley D, Sol-Church K, Timms AE, Dobyns WB.

Am J Med Genet A. 2016 Sep;170(9):2237-47. doi: 10.1002/ajmg.a.37781. Epub 2016 Jun 5.

11.

Loose anagen hair syndrome: Is there any association with atopic dermatitis?

Dey VK, Thawani M.

Indian Dermatol Online J. 2016 Jan-Feb;7(1):56-7. doi: 10.4103/2229-5178.174309. No abstract available.

12.

Loose Anagen Hair Syndrome.

Srinivas SM.

Int J Trichology. 2015 Jul-Sep;7(3):138-9. doi: 10.4103/0974-7753.167467. No abstract available.

13.

Cardiomyopathies in Noonan syndrome and the other RASopathies.

Gelb BD, Roberts AE, Tartaglia M.

Prog Pediatr Cardiol. 2015 Jul 1;39(1):13-19.

14.

Hair loss in children.

Alves R, Grimalt R.

Curr Probl Dermatol. 2015;47:55-66. doi: 10.1159/000369405. Epub 2015 Feb 20. Review.

PMID:
26370644
15.

N(1)-methylspermidine, a stable spermidine analog, prolongs anagen and regulates epithelial stem cell functions in human hair follicles.

Ramot Y, Marzani B, Pinto D, Kloepper JE, Paus R.

Arch Dermatol Res. 2015 Nov;307(9):841-7. doi: 10.1007/s00403-015-1592-9. Epub 2015 Jul 28.

PMID:
26216444
16.

Improved growth velocity of a patient with Noonan-like syndrome with loose anagen hair (NS/LAH) without growth hormone deficiency by low-dose growth hormone therapy.

Takasawa K, Takishima S, Morioka C, Nishioka M, Ohashi H, Aoki Y, Shimohira M, Kashimada K, Morio T.

Am J Med Genet A. 2015 Oct;167A(10):2425-9. doi: 10.1002/ajmg.a.37191. Epub 2015 Jun 19.

PMID:
26096762
17.

Trichoscopy findings in loose anagen hair syndrome: rectangular granular structures and solitary yellow dots.

Rakowska A, Zadurska M, Czuwara J, Warszawik-Hendzel O, Kurzeja M, Maj M, Olszewska M, Rudnicka L.

J Dermatol Case Rep. 2015 Mar 31;9(1):1-5. doi: 10.3315/jdcr.2015.1193. eCollection 2015 Mar 31.

18.

PTPN11 mutation manifesting as LEOPARD syndrome associated with hypertrophic plexi and neuropathic pain.

Spatola M, Wider C, Kuntzer T, Croquelois A.

BMC Neurol. 2015 Apr 16;15:55. doi: 10.1186/s12883-015-0310-8.

19.

Moyamoya disease in two patients with Noonan-like syndrome with loose anagen hair.

Lo FS, Wang CJ, Wong MC, Lee NC.

Am J Med Genet A. 2015 Jun;167(6):1285-8. doi: 10.1002/ajmg.a.37053. Epub 2015 Apr 9.

PMID:
25858597
20.

Noonan syndrome-like disorder with loose anagen hair: a second case with neuroblastoma.

Garavelli L, Cordeddu V, Errico S, Bertolini P, Street ME, Rosato S, Pollazzon M, Wischmeijer A, Ivanovski I, Daniele P, Bacchini E, Lombardi AA, Izzi G, Biasucci G, Del Rossi C, Corradi D, Cazzaniga G, Dominici C, Rossi C, De Luca A, Bernasconi S, Riccardi R, Legius E, Tartaglia M.

Am J Med Genet A. 2015 Aug;167A(8):1902-7. doi: 10.1002/ajmg.a.37082. Epub 2015 Apr 5.

PMID:
25846317

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