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congenital fecial atrophy相关文献:
Facial dysmorphism in congenital rubella syndrome.
Chattannavar G, Bansal A, Kekunnaya R.
J AAPOS. 2024 Feb;28(1):103791. doi: 10.1016/j.jaapos.2023.08.020. Epub 2023 Nov 7.
PMID:37939916
NSDHL-Related Disorders.
Kurban M, El Feghaly J, Hamie L.
2011 Feb 1 [updated 2024 Sep 5]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:21290788
Chiari-like Malformation.
Loughin CA.
Vet Clin North Am Small Anim Pract. 2016 Mar;46(2):231-42. doi: 10.1016/j.cvsm.2015.10.002. Epub 2015 Nov 27.
PMID:26631589
Crouzon Syndrome.
Zeppieri M, Karsonovich T, Patel BC.
2025 May 25. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–.
PMID:30085540
Fukuyama Congenital Muscular Dystrophy.
Saito K.
2006 Jan 26 [updated 2025 May 8]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:20301385
Neu Laxova syndrome.
Dwivedi T, Gosavi M.
Indian J Pathol Microbiol. 2019 Jan-Mar;62(1):149-152. doi: 10.4103/IJPM.IJPM_351_17.
PMID:30706883
[Congenital myopathies].
Cabello A, Ricoy-Campo JR.
Rev Neurol. 2003 Oct 16-31;37(8):779-86.
PMID:14593641
Epiphora.
Patel J, Levin A, Patel BC.
2023 Aug 7. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–.
PMID:32491381
Progression of cerebral and cerebellar atrophy in congenital contractures of limbs and face, hypotonia, and developmental delay.
Kumaki T, Enomoto Y, Aida N, Goto T, Kurosawa K.
Pediatr Int. 2022 Jan;64(1):e14734. doi: 10.1111/ped.14734. Epub 2021 Oct 29.
PMID:34714572
Ptosis Correction.
Koka K, Patel BC.
2023 Jul 10. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–.
PMID:30969650
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