229 related articles for article (PubMed ID: 14113527)
1. [ON A FAMILY WITH THE RECESSIVE TRAIT OF WOOLLY HAIR, HYPOTRICHOSIS AND OTHER ANOMALIES].
SALAMON T
Hautarzt; 1963 Dec; 14():540-4. PubMed ID: 14113527
[No Abstract] [Full Text] [Related]
2. Bimatoprost for the treatment of eyelash, eyebrow and scalp alopecia.
Barrón-Hernández YL; Tosti A
Expert Opin Investig Drugs; 2017 Apr; 26(4):515-522. PubMed ID: 28264599
[TBL] [Abstract][Full Text] [Related]
3. Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan.
Khan S; Habib R; Mir H; Umm-e-Kalsoom ; Naz G; Ayub M; Shafique S; Yamin T; Ali N; Basit S; Wasif N; Kamran-Ul-Hassan Naqvi S; Ali G; Wali A; Ansar M; Ahmad W
Clin Exp Dermatol; 2011 Aug; 36(6):652-4. PubMed ID: 21426374
[TBL] [Abstract][Full Text] [Related]
4. Mutations in the lipase-H gene causing autosomal recessive hypotrichosis and woolly hair.
Mehmood S; Jan A; Muhammad D; Ahmad F; Mir H; Younus M; Ali G; Ayub M; Ansar M; Ahmad W
Australas J Dermatol; 2015 Aug; 56(3):e66-70. PubMed ID: 24628704
[TBL] [Abstract][Full Text] [Related]
5. Hereditary ciliary and superciliary hypotrichosis of a dominant character.
URRETS-ZAVALIA A; JIMENEZ ES
Br J Ophthalmol; 1958 Nov; 42(11):694-6. PubMed ID: 13596561
[No Abstract] [Full Text] [Related]
6. Ciliary and superciliary hypotrichosis. A distinct autosomal dominant trait.
García-Esquivel L; Hernández A; Reynoso MC; Fragoso R; Villar-Calvo VM; Soto F; Cantú JM
Ophthalmic Paediatr Genet; 1986 Aug; 7(2):77-9. PubMed ID: 3785882
[TBL] [Abstract][Full Text] [Related]
7. CONGENITAL CILIARY HYPOTRICHOSIS.
SARDA RP; CHARAN H; NAGPAUL PN
Ophthalmologica; 1964; 148():365-6. PubMed ID: 14269085
[No Abstract] [Full Text] [Related]
8. Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles.
Zernov NV; Skoblov MY; Marakhonov AV; Shimomura Y; Vasilyeva TA; Konovalov FA; Abrukova AV; Zinchenko RA
J Invest Dermatol; 2016 Jun; 136(6):1097-1105. PubMed ID: 26902920
[TBL] [Abstract][Full Text] [Related]
9. Non-syndromic hypotrichosis: A report of two novel variants in the LSS gene.
El Hakim J; Mehawej C; Chouery E; Megarbane A; El-Feghaly J; El Khoury J
Pediatr Dermatol; 2023; 40(5):960-961. PubMed ID: 37029088
[TBL] [Abstract][Full Text] [Related]
10. Marie Unna hereditary hypotrichosis: a Turkish family with loss of eyebrows and a U2HR mutation.
Mansur AT; Elcioglu NH; Redler S; Serdar ZA; Cetinel S; Betz RC; Akarsu NA
Am J Med Genet A; 2010 Oct; 152A(10):2628-33. PubMed ID: 20814945
[TBL] [Abstract][Full Text] [Related]
11. Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex.
Romano MT; Tafazzoli A; Mattern M; Sivalingam S; Wolf S; Rupp A; Thiele H; Altmüller J; Nürnberg P; Ellwanger J; Gambon R; Baumer A; Kohlschmidt N; Metze D; Holdenrieder S; Paus R; Lütjohann D; Frank J; Geyer M; Bertolini M; Kokordelis P; Betz RC
Am J Hum Genet; 2018 Nov; 103(5):777-785. PubMed ID: 30401459
[TBL] [Abstract][Full Text] [Related]
12. Mutational analysis of 29 patients with autosomal-recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal-recessive woolly hair and hypotrichosis in Japan.
Takeichi T; Tanahashi K; Taki T; Kono M; Sugiura K; Akiyama M
Br J Dermatol; 2017 Jul; 177(1):290-292. PubMed ID: 27641630
[No Abstract] [Full Text] [Related]
13. Alopecia in genetic diseases.
Calvieri S; Rossi A
G Ital Dermatol Venereol; 2014 Feb; 149(1):1-13. PubMed ID: 24566562
[TBL] [Abstract][Full Text] [Related]
14. Hereditary hypotrichosis. A previously undescribed syndrome.
Bentley-Phillips B; Grace HJ
Br J Dermatol; 1979 Sep; 101(3):331-9. PubMed ID: 508598
[TBL] [Abstract][Full Text] [Related]
15. Hair transplantation to the eyebrow, eyelashes, and other parts of the body.
Gandelman M; Epstein JS
Facial Plast Surg Clin North Am; 2004 May; 12(2):253-61. PubMed ID: 15135136
[TBL] [Abstract][Full Text] [Related]
16. Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype.
Avrahami L; Maas S; Pasmanik-Chor M; Rainshtein L; Magal N; Smitt J; van Marle J; Shohat M; Basel-Vanagaite L
Clin Genet; 2008 Jul; 74(1):47-53. PubMed ID: 18445049
[TBL] [Abstract][Full Text] [Related]
17. Novel small-insertion mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis.
Lv H; Li M; Cheng R
J Dermatol; 2020 Dec; 47(12):1445-1449. PubMed ID: 32901930
[TBL] [Abstract][Full Text] [Related]
18. [THE WHITE FORELOCK AND MYOPIA AS "INDICATOR" FACTORS OF THE WAARDENBURG-KLEIN SYNDROME].
COUTEAU-LAGARDE JM; COLLIER M
J Genet Hum; 1963 Dec; 12():146-53. PubMed ID: 14136826
[No Abstract] [Full Text] [Related]
19. Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous families.
Ahmad F; Sharif S; Furqan Ubaid M; Shah K; Khan MN; Umair M; Azeem Z; Ahmad W
Congenit Anom (Kyoto); 2018 Jan; 58(1):24-28. PubMed ID: 28425126
[TBL] [Abstract][Full Text] [Related]
20. Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotype.
Shah SH; Abid A; Shahid S; Khaliq S
J Pak Med Assoc; 2011 Nov; 61(11):1060-4. PubMed ID: 22125978
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]