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familial short stature相关文献:
Evaluation of Short Stature in Children and Adolescents.
Patel R, Bajpai A.
Indian J Pediatr. 2021 Dec;88(12):1196-1202. doi: 10.1007/s12098-021-03880-9. Epub 2021 Aug 16.
PMID:34398416
Definition and prevalence of familial short stature.
Grigoletto V, Occhipinti AA, Pellegrin MC, Sirchia F, Barbi E, Tornese G.
Ital J Pediatr. 2021 Mar 9;47(1):56. doi: 10.1186/s13052-021-01018-3.
PMID:33750447
Genetic Architecture Associated With Familial Short Stature.
Lin YJ, Cheng CF, Wang CH, Liang WM, Tang CH, Tsai LP, Chen CH, Wu JY, Hsieh AR, Lee MTM, Lin TH, Liao CC, Huang SM, Zhang Y, Tsai CH, Tsai FJ.
J Clin Endocrinol Metab. 2020 Jun 1;105(6):dgaa131. doi: 10.1210/clinem/dgaa131.
PMID:32170311
Novel heterozygous mutation in the SHOX gene leading to familial idiopathic short stature: A case report and literature review.
Liu L, Li J, Li J, Hu H, Liu J, Tang P.
Medicine (Baltimore). 2023 Oct 13;102(41):e35471. doi: 10.1097/MD.0000000000035471.
PMID:37832088
Approach to short stature.
Yadav S, Dabas A.
Indian J Pediatr. 2015 May;82(5):462-70. doi: 10.1007/s12098-014-1609-y. Epub 2014 Dec 4.
PMID:25465677
Burden and Treatment of Achondroplasia: A Systematic Literature Review.
Murton MC, Drane ELA, Goff-Leggett DM, Shediac R, O'Hara J, Irving M, Butt TJ.
Adv Ther. 2023 Sep;40(9):3639-3680. doi: 10.1007/s12325-023-02549-3. Epub 2023 Jun 29.
PMID:37382866
Short Stature due to Bioinactive Growth Hormone (Kowarski Syndrome).
Karaoglan M.
Endocr Pract. 2023 Nov;29(11):902-911. doi: 10.1016/j.eprac.2023.08.013. Epub 2023 Aug 30.
PMID:37657628
Orthopedic concerns of a child with short stature.
Liau ZQG, Wang Y, Lin HY, Cheong CK, Gupta S, Hui JHP.
Curr Opin Pediatr. 2022 Feb 1;34(1):82-91. doi: 10.1097/MOP.0000000000001081.
PMID:34840250
The Treatment of Growth Disorders in Childhood and Adolescence.
Woelfle J, Schnabel D, Binder G.
Dtsch Arztebl Int. 2024 Feb 9;121(3):96-106. doi: 10.3238/arztebl.m2023.0247.
PMID:38051162
Familial spherophakia with short stature caused by a novel homozygous ADAMTS17 mutation.
Khan AO, Aldahmesh MA, Al-Ghadeer H, Mohamed JY, Alkuraya FS.
Ophthalmic Genet. 2012 Dec;33(4):235-9. doi: 10.3109/13816810.2012.666708. Epub 2012 Apr 9.
PMID:22486325
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