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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 2 |
2020 | 2 |
2021 | 1 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
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Page 1
The incidence and mortality rate of catheter-related neonatal pericardial effusion: A meta-analysis.
Medicine (Baltimore). 2022 Nov 25;101(47):e32050. doi: 10.1097/MD.0000000000032050.
Medicine (Baltimore). 2022.
PMID: 36451499
Free PMC article.
Transcriptome analysis unveils the mechanisms of lipid metabolism response to grayanotoxin I stress in Spodoptera litura.
Zhou Y, Wu YM, Fan R, Ouyang J, Zhou XL, Li ZB, Janjua MU, Li HG, Bao MH, He BS.
Zhou Y, et al. Among authors: janjua mu.
PeerJ. 2023 Dec 6;11:e16238. doi: 10.7717/peerj.16238. eCollection 2023.
PeerJ. 2023.
PMID: 38077416
Free PMC article.
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Detailed analysis of Ethereum network on transaction behavior, community structure and link prediction.
Said A, Janjua MU, Hassan SU, Muzammal Z, Saleem T, Thaipisutikul T, Tuarob S, Nawaz R.
Said A, et al. Among authors: janjua mu.
PeerJ Comput Sci. 2021 Dec 10;7:e815. doi: 10.7717/peerj-cs.815. eCollection 2021.
PeerJ Comput Sci. 2021.
PMID: 34977356
Free PMC article.
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Putative Digenic GJB2/MYO7A Inheritance of Hearing Loss Detected in a Patient with 48,XXYY Klinefelter Syndrome.
Zhang Q, Qin T, Hu W, Janjua MU, Jin P.
Zhang Q, et al. Among authors: janjua mu.
Hum Hered. 2020;85(3-6):117-124. doi: 10.1159/000516854. Epub 2021 Jun 30.
Hum Hered. 2020.
PMID: 34192699
Free PMC article.
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Identification of two novel mutations in three Chinese families with Kallmann syndrome using whole exome sequencing.
Zhang Q, He HH, Janjua MU, Wang F, Yang YB, Mo ZH, Liu J, Jin P.
Zhang Q, et al. Among authors: janjua mu.
Andrologia. 2020 Aug;52(7):e13594. doi: 10.1111/and.13594. Epub 2020 May 12.
Andrologia. 2020.
PMID: 32400067
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Association of medullary sponge kidney and hyperparathyroidism with RET G691S/S904S polymorphism: a case report.
Janjua MU, Long XD, Mo ZH, Dong CS, Jin P.
Janjua MU, et al.
J Med Case Rep. 2018 Jul 9;12(1):197. doi: 10.1186/s13256-018-1736-6.
J Med Case Rep. 2018.
PMID: 29983117
Free PMC article.
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Extensive ARMC5 genetic variance in primary bilateral macronodular adrenal hyperplasia that started with exophthalmos: a case report.
Jin P, Janjua MU, Zhang Q, Dong CS, Yang Y, Mo ZH.
Jin P, et al. Among authors: janjua mu.
J Med Case Rep. 2018 Jan 18;12(1):13. doi: 10.1186/s13256-017-1529-3.
J Med Case Rep. 2018.
PMID: 29343284
Free PMC article.
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