BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 24696032)

  • 1. CHILD syndrome: effective treatment of ichthyosiform naevus with oral and topical ketoconazole.
    Liu T; Qian G; Wang XX; Zhang YG
    Acta Derm Venereol; 2015 Jan; 95(1):91-2. PubMed ID: 24696032
    [No Abstract]   [Full Text] [Related]  

  • 2. A novel X-chromosomal microdeletion encompassing congenital hemidysplasia with ichthyosiform erythroderma and limb defects.
    Raychaudhury T; George R; Mandal K; Srivastava VM; Thomas M; Bornholdt D; Grzeschik KH; Koehler A
    Pediatr Dermatol; 2013; 30(2):250-2. PubMed ID: 22471832
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mild clinical presentation of a patient with a mutation in the NSDHL gene.
    Ormerod E; Bownass L; Smithson S; Zhang Y; Dunnill MGS
    Clin Exp Dermatol; 2019 Jun; 44(4):456-458. PubMed ID: 30488480
    [No Abstract]   [Full Text] [Related]  

  • 4. CHILD syndrome: successful treatment of skin lesions with topical lovastatin and cholesterol lotion.
    Sandoval KR; Machado MCR; Oliveira ZNP; Nico MMS
    An Bras Dermatol; 2019 Jul; 94(3):341-343. PubMed ID: 31365666
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Skin Abnormalities in CHILD Syndrome Successfully Treated with Pathogenesis-based Therapy.
    Christiansen AG; Koppelhus U; Sommerlund M
    Acta Derm Venereol; 2015 Jul; 95(6):752-3. PubMed ID: 25587692
    [No Abstract]   [Full Text] [Related]  

  • 6. Novel
    Maceda EBG; Kratz LE; Ramos VME; Abacan MAR
    BMJ Case Rep; 2020 Nov; 13(11):. PubMed ID: 33139364
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CHILD syndrome mimicking verrucous nevus in a Chinese patient responded well to the topical therapy of compound of simvastatin and cholesterol.
    Yu X; Zhang J; Gu Y; Deng D; Wu Z; Bao L; Li M; Yao Z
    J Eur Acad Dermatol Venereol; 2018 Jul; 32(7):1209-1213. PubMed ID: 29341259
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CHILD syndrome with mild skin lesions: histopathologic clues for the diagnosis.
    Gantner S; Rütten A; Requena L; Gassenmaier G; Landthaler M; Hafner C
    J Cutan Pathol; 2014 Oct; 41(10):787-90. PubMed ID: 25093865
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An excellent response to topical therapy of four congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome patients with an increased concentration of simvastatin ointment.
    Yu X; Chen L; Yang Z; Gu Y; Zheng W; Wu Z; Li M; Yao Z
    J Eur Acad Dermatol Venereol; 2020 Jan; 34(1):e8-e11. PubMed ID: 31374135
    [No Abstract]   [Full Text] [Related]  

  • 10. Large deletions in the NSDHL gene in two patients with CHILD syndrome.
    Yang Z; Hartmann B; Xu Z; Ma L; Happle R; Schlipf N; Zhang LX; Xu ZG; Wang ZY; Fischer J
    Acta Derm Venereol; 2015 Nov; 95(8):1007-8. PubMed ID: 26014843
    [No Abstract]   [Full Text] [Related]  

  • 11. CHILD Syndrome: Successful Treatment of Skin Lesions with Topical Simvastatin/Cholesterol Ointment--A Case Report.
    Alexopoulos A; Kakourou T
    Pediatr Dermatol; 2015; 32(4):e145-7. PubMed ID: 25845514
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CHILD syndrome: A modified pathogenesis-targeted therapeutic approach.
    Bergqvist C; Abdallah B; Hasbani DJ; Abbas O; Kibbi AG; Hamie L; Kurban M; Rubeiz N
    Am J Med Genet A; 2018 Mar; 176(3):733-738. PubMed ID: 29392821
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next-generation sequencing causes CK syndrome.
    Preiksaitiene E; Caro A; Benušienė E; Oltra S; Orellana C; Morkūnienė A; Roselló MP; Kasnauskiene J; Monfort S; Kučinskas V; Mayo S; Martinez F
    Am J Med Genet A; 2015 Jun; 167(6):1342-8. PubMed ID: 25900314
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CHILD syndrome with minimal limb abnormalities.
    Noguera-Morel L; Hernández-Ostiz S; Casas-Fernández L; Hernández-Martín A; Rodríguez-Blanco I; Requena L; Hotz A; Fischer J; Torrelo A
    J Eur Acad Dermatol Venereol; 2016 Dec; 30(12):e201-e202. PubMed ID: 26611379
    [No Abstract]   [Full Text] [Related]  

  • 15. CHILD syndrome caused by a deletion of exons 6-8 of the NSDHL gene.
    Kim CA; Konig A; Bertola DR; Albano LM; Gattás GJ; Bornholdt D; Leveleki L; Happle R; Grzeschik KH
    Dermatology; 2005; 211(2):155-8. PubMed ID: 16088165
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital hemidysplasia with ichthyosiform naevus and limb defects (CHILD) syndrome without hemidysplasia.
    Estapé A; Josifova D; Rampling D; Glover M; Kinsler VA
    Br J Dermatol; 2015 Jul; 173(1):304-7. PubMed ID: 25533639
    [No Abstract]   [Full Text] [Related]  

  • 17. CHILD syndrome.
    Heda GD; Valivade V; Sanghavi P; Kukreja RM; Phulari YJ
    Indian J Dermatol Venereol Leprol; 2014; 80(5):483. PubMed ID: 25201868
    [No Abstract]   [Full Text] [Related]  

  • 18. CHILD Syndrome: Case Report of a Chinese Patient and Literature Review of the NAD[P]H Steroid Dehydrogenase-Like Protein Gene Mutation.
    Mi XB; Luo MX; Guo LL; Zhang TD; Qiu XW
    Pediatr Dermatol; 2015; 32(6):e277-82. PubMed ID: 26459993
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Brain and cerebellar hemidysplasia in a case with ipsilateral body dysplasia and suspicion of CHILD syndrome.
    Schmidt-Sidor B; Obersztyn E; Szymańska K; Wychowski J; Mierzewska H; Wierzba-Bobrowicz T; Stepień T
    Folia Neuropathol; 2008; 46(3):232-7. PubMed ID: 18825599
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tympanoxyloid verruciform xanthoma is a distinct feature of CHILD nevus.
    Juratli HA; König A; Happle R
    J Eur Acad Dermatol Venereol; 2020 Feb; 34(2):e70-e72. PubMed ID: 31502355
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.