These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

224 related items for 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.
    ; . PubMed ID:
    [No 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
    [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
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. CONGENITAL CILIARY HYPOTRICHOSIS.
    SARDA RP, CHARAN H, NAGPAUL PN.
    Ophthalmologica; 1964 Aug; 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
    [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 Jun; 40(5):960-961. PubMed ID: 37029088
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No 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
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No 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
    [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
    [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
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.