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congenital ectodermal dysplasia 相关文献:
Congenital ectodermal dysplasia.
DODS L.
Med J Aust. 1946 Jun 8;1(23):815. doi: 10.5694/j.1326-5377.1935.tb77475.x.
PMID:21064988
Ankyloblepharon-ectodermal dysplasia-clefting syndrome misdiagnosed as epidermolysis bullosa and congenital ichthyosiform erythroderma: Case report and review of published work.
Zhang Z, Cheng R, Liang J, Lu Z, Wang Y, Li M, Yu H, Yao Z.
J Dermatol. 2019 May;46(5):422-425. doi: 10.1111/1346-8138.14837. Epub 2019 Feb 27.
PMID:30809829
Increased intracranial pressure in a patient with Congenital Heart Defect and Ectodermal Dysplasia (CHDED): Extension of phenotype and review of literature.
Alghaith FA, Arts HH, Plourde FJ, Boswall A, Gulati P, McNeely PD, Acott PD, Wong KK, Dyack S.
Am J Med Genet A. 2023 Feb;191(2):554-558. doi: 10.1002/ajmg.a.63023. Epub 2022 Oct 29.
PMID:36308391
Congenital ectodermal dysplasia.
GREGORY ID.
Br J Ophthalmol. 1955 Jan;39(1):44-7. doi: 10.1136/bjo.39.1.44.
PMID:13230426
Congenital ectodermal dysplasia.
SPIRA L.
Acta Med Scand. 1947 May 17;127(6):570-600. doi: 10.1111/j.0954-6820.1947.tb13169.x.
PMID:20247962
Congenital ectodermal dysplasia.
Naqvi AN.
J Pak Med Assoc. 1985 Jul;35(7):225-7.
PMID:3930781
Ectodermal dysplasia with congenital adermatoglyphia (Basan syndrome): Report of two cases presenting with extensive congenital milia.
Nieto-Benito LM, Molina-López I, Feito-Rodríguez M, Martínez-González V, Suárez-Fernández R, Campos-Dominguez M.
Pediatr Dermatol. 2021 Mar;38(2):530-532. doi: 10.1111/pde.14512. Epub 2021 Jan 24.
PMID:33486784
Ocular manifestations of ectodermal dysplasia.
Landau Prat D, Katowitz WR, Strong A, Katowitz JA.
Orphanet J Rare Dis. 2021 May 1;16(1):197. doi: 10.1186/s13023-021-01824-2.
PMID:33933124
Congenital nail abnormalities.
Nahmani L, Fitoussi F.
Hand Surg Rehabil. 2024 Apr;43S:101527. doi: 10.1016/j.hansur.2023.01.011.
PMID:38879228
Congenital Nail Disorders among Children with Suspected Ectodermal Dysplasias.
Maier-Wohlfart S, Aicher C, Willershausen I, Peschel N, Meißner U, Gölz L, Schneider H.
Genes (Basel). 2022 Nov 15;13(11):2119. doi: 10.3390/genes13112119.
PMID:36421794
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