Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 76

Similar articles for PubMed (Select 17656942)

1.

Monilethrix.

Narmatha GR, Chithra S, Balasubramanian N.

Indian J Dermatol Venereol Leprol. 2002 Jul-Aug;68(4):220-1.

2.

Monilethrix: a rare hereditary condition.

Vikramkumar AG, Kuruvila S, Ganguly S.

Indian J Dermatol. 2013 May;58(3):243. doi: 10.4103/0019-5154.110869.

3.

Monilethrix--improvement by hormonal influences?

Gebhardt M, Fischer T, Claussen U, Wollina U, Elsner P.

Pediatr Dermatol. 1999 Jul-Aug;16(4):297-300.

PMID:
10469416
4.

Monilethrix: a typical case report with microscopic and dermatoscopic findings.

Oliveira EF, Araripe AL.

An Bras Dermatol. 2015 Jan-Feb;90(1):126-7. doi: 10.1590/abd1806-4841.20153357.

5.

Hereditary leukonychia totalis, acanthosis-nigricans-like lesions and hair dysplasia: a new syndrome?

Le Corre Y, Steff M, Croue A, Filmon R, Verret JL, Le Clech C.

Eur J Med Genet. 2009 Jul-Aug;52(4):229-33. doi: 10.1016/j.ejmg.2009.04.003. Epub 2009 May 4.

PMID:
19401242
6.

Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.

Celep F, Uzumcu A, Sonmez FM, Uyguner O, Balci YI, Bahadir S, Karaguzel A.

Genet Couns. 2009;20(1):1-8.

PMID:
19400537
7.

Additional familial case of subtotal leukonychia and sebaceous cysts (Bauer syndrome): belong the nervous tumours to the phenotype?

Morin G, Desenclos C, Jeanpetit C, Lévy N, Deramond H, Mathieu M.

Eur J Med Genet. 2008 Sep-Oct;51(5):436-43. doi: 10.1016/j.ejmg.2008.05.004. Epub 2008 May 28.

PMID:
18684681
8.

Monilethrix, a rare inherited hair shaft disorder in siblings.

Vora RV, Anjaneyan G, Mehta MJ.

Indian Dermatol Online J. 2014 Jul;5(3):339-40. doi: 10.4103/2229-5178.137795. No abstract available.

9.

A case for diagnosis; monilethrix?

SCHEER M.

Arch Derm Syphilol. 1948 Mar;57(3 Pt. 2):554. No abstract available.

PMID:
18098710
10.

A case of rare recessive oculopharyngeal muscular dystrophy (OPMD) coexisting with hereditary neuropathy with liability to pressure palsies (HNPP).

Marsh EA, Robinson DO.

Clin Neurol Neurosurg. 2008 May;110(5):525-8. doi: 10.1016/j.clineuro.2008.02.007. Epub 2008 Mar 21.

PMID:
18358598
11.

Monilethrix.

de Lencastre A, Tosti A.

J Pediatr. 2012 Dec;161(6):1176. doi: 10.1016/j.jpeds.2012.06.033. Epub 2012 Aug 9. No abstract available.

PMID:
22884362
12.

Hereditary persistence of alpha-fetoprotein.

Li X, Alexander S.

Pediatr Blood Cancer. 2009 Mar;52(3):403-5. doi: 10.1002/pbc.21816.

PMID:
18985745
13.
14.

[Analysis of human hair basic keratin 6 gene mutation in a Chinese Han family with monilethrix].

Feng AP, Liu P, Yang T.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Apr;25(2):141-4. Chinese.

PMID:
18393232
15.

Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.

Schüle R, Bonin M, Dürr A, Forlani S, Sperfeld AD, Klimpe S, Mueller JC, Seibel A, van de Warrenburg BP, Bauer P, Schöls L.

Neurology. 2009 Jun 2;72(22):1893-8. doi: 10.1212/WNL.0b013e3181a6086c. Epub 2009 Apr 8.

PMID:
19357379
16.

[Hereditary non-polyposis colorectal cancer. Report of four siblings].

Zárate A, Alvarez K, Wielandt AM, Hevia M, De la Fuente M, Carvallo P, López-Köstner F.

Rev Med Chil. 2008 Jun;136(6):757-62. doi: /S0034-98872008000600011. Epub 2008 Aug 26. Spanish.

17.

Osler-Weber-Rendu syndrome: a case report with familial clustering.

Grover S, Grewal RS, Verma R, Sahni H, Muralidhar R, Sinha P.

Indian J Dermatol Venereol Leprol. 2009 Jan-Feb;75(1):100-1.

18.

Hereditary optic neuropathies share a common mitochondrial coupling defect.

Chevrollier A, Guillet V, Loiseau D, Gueguen N, de Crescenzo MA, Verny C, Ferre M, Dollfus H, Odent S, Milea D, Goizet C, Amati-Bonneau P, Procaccio V, Bonneau D, Reynier P.

Ann Neurol. 2008 Jun;63(6):794-8. doi: 10.1002/ana.21385.

PMID:
18496845
19.

Early onset of hereditary gingival fibromatosis in a 28-month-old.

Breen GH, Addante R, Black CC.

Pediatr Dent. 2009 Jul-Aug;31(4):286-8.

PMID:
19722435
20.

A new corneal disease with recurrent erosive episodes and autosomal-dominant inheritance.

Hammar B, Björck E, Lagerstedt K, Dellby A, Fagerholm P.

Acta Ophthalmol. 2008 Nov;86(7):758-63. doi: 10.1111/j.1600-0420.2007.01123.x. Epub 2008 Sep 5.

PMID:
18778339
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk