首页 > 按专业查询名词 > 查询PubMed相关文献
名词信息
Pubmed相关的文献
head foruncle相关文献:
Retinal detachment in Loeys-Dietz syndrome.
Maghsoudi D, Nixon TRW, Snead MP.
Am J Med Genet A. 2023 Mar;191(3):846-849. doi: 10.1002/ajmg.a.63077. Epub 2022 Dec 18.
PMID:36529632
Hereditary paraganglioma.
Lemaire M, Persu A, Hainaut P, De Plaen JF.
J Intern Med. 1999 Jul;246(1):113-6. doi: 10.1046/j.1365-2796.1999.00519.x.
PMID:10447233
Trauma and hyperactivity: differentiating symptoms and cause.
Arunyanart W, Weitzman C, Groves B, Augustyn M.
J Dev Behav Pediatr. 2011 Jul-Aug;32(6):482-4. doi: 10.1097/DBP.0b013e318221b6a8.
PMID:21654333
An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature.
Trippella G, Lionetti P, Naldini S, Peluso F, Monica MD, Stagi S.
Ital J Pediatr. 2018 Nov 20;44(1):138. doi: 10.1186/s13052-018-0580-z.
PMID:30458885
X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second family.
Lungarotti MS, Martello C, Barboni G, Mezzetti D, Mariotti G, Calabro A.
Am J Med Genet. 1994 Jul 15;51(4):598-601. doi: 10.1002/ajmg.1320510460.
PMID:7943046
Quality of life after total laryngectomy: functioning, psychological well-being and self-efficacy.
Perry A, Casey E, Cotton S.
Int J Lang Commun Disord. 2015 Jul;50(4):467-75. doi: 10.1111/1460-6984.12148. Epub 2015 Feb 19.
PMID:25703153
A novel de novo TP63 mutation in whole-exome sequencing of a Syrian family with Oral cleft and ectrodactyly.
Simpson CL, Kimble DC, Chandrasekharappa SC; NISC Comparative Sequencing Program; Alqosayer K, Holzinger E, Carrington B, McElderry J, Sood R, Al-Souqi G, Albacha-Hejazi H, Bailey-Wilson JE.
Mol Genet Genomic Med. 2023 Aug;11(8):e2179. doi: 10.1002/mgg3.2179. Epub 2023 Apr 18.
PMID:37070724
Pseudodominant Nanophthalmos in a Roma Family Caused by a Novel PRSS56 Variant.
Dudakova L, Skalicka P, Ulmanová O, Hlozanek M, Stranecky V, Malinka F, Vincent AL, Liskova P.
J Ophthalmol. 2020 May 10;2020:6807809. doi: 10.1155/2020/6807809. eCollection 2020.
PMID:32454992
"Footprints in the Bathroom": The Role of Spirituality in Patient Diagnosis.
Meneses V, Vanderbilt D, Barnes L, Augustyn M.
J Dev Behav Pediatr. 2017 Feb/Mar;38 Suppl 1:S79-S81. doi: 10.1097/DBP.0000000000000393.
PMID:28141730
A case of alpha-synuclein gene duplication presenting with head-shaking movements.
Itokawa K, Sekine T, Funayama M, Tomiyama H, Fukui M, Yamamoto T, Tamura N, Matsuda H, Hattori N, Araki N.
Mov Disord. 2013 Mar;28(3):384-7. doi: 10.1002/mds.25243. Epub 2012 Nov 2.
PMID:23124679
© Copyright 2021 鸿泰茂源  版权所有All Rights Reserved京ICP备11040441号-3