Found: 7
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Atypical phenotypes and novel OCRL variations in southern Chinese patients with Lowe syndrome.
- Published in:
- Pediatric Nephrology, 2024, v. 39, n. 8, p. 2377, doi. 10.1007/s00467-024-06356-y
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- Publication type:
- Article
The EGFR‐P38 MAPK axis up‐regulates PD‐L1 through miR‐675‐5p and down‐regulates HLA‐ABC via hexokinase‐2 in hepatocellular carcinoma cells.
- Published in:
- Cancer Communications, 2021, v. 41, n. 1, p. 62, doi. 10.1002/cac2.12117
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- Publication type:
- Article
Features of BSCL2 related congenital generalized lipodystrophy in China: long-term follow-up of three patients and literature review.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2023, v. 36, n. 1, p. 74, doi. 10.1515/jpem-2022-0372
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- Publication type:
- Article
Novel TTV variants isolated in an epidemic of hepatitis of unknown etiology.
- Published in:
- Journal of Medical Virology, 2002, v. 67, n. 1, p. 113, doi. 10.1002/jmv.2199
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- Publication type:
- Article
A very rare case report of glycogen storage disease type IXc with novel PHKG2 variants.
- Published in:
- 2022
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- Publication type:
- journal article
Clinical characteristics and prognosis of early diagnosed Wilson's disease: A large cohort study.
- Published in:
- Liver International, 2024, v. 44, n. 9, p. 2424, doi. 10.1111/liv.16009
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- Publication type:
- Article
Modified nusinersen intrathecal injection method: inclusion of a septal needle-free closed infusion connector.
- Published in:
- Frontiers in Neurology, 2023, p. 01, doi. 10.3389/fneur.2023.1234442
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- Publication type:
- Article