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Correction: One-stop combined CT angiography of coronary and craniocervical arteries: recommended as the first examination for patients suspected of coronary or craniocervical artery disease.
- Published in:
- European Radiology, 2023, v. 33, n. 10, p. 7352, doi. 10.1007/s00330-023-09981-7
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- Article
One-stop combined CT angiography of coronary and craniocervical arteries: recommended as the first examination for patients suspected of coronary or craniocervical artery disease.
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- European Radiology, 2023, v. 33, n. 10, p. 7034, doi. 10.1007/s00330-023-09528-w
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- Article
Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma.
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- Cellular Physiology & Biochemistry (Karger AG), 2018, v. 46, n. 5, p. 1919, doi. 10.1159/000489381
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- Article
High-resolution oblique coronal MRI at optimal flexed-knee angle: a novel imaging method for enhanced anterior cruciate ligament tear diagnosis.
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- Journal of Orthopaedic Surgery & Research, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13018-024-04956-w
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- Article
Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss.
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- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0136306
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- Article
Novel and Recurring NOTCH3 Mutations in Two Chinese Patients with CADASIL.
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- Neurodegenerative Diseases, 2019, v. 19, n. 1, p. 35, doi. 10.1159/000500166
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- Article
Identification of a GNE homozygous mutation in a Han‐Chinese family with GNE myopathy.
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- Journal of Cellular & Molecular Medicine, 2018, v. 22, n. 11, p. 5533, doi. 10.1111/jcmm.13827
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- Article
Compound heterozygous POMT1 mutations in a Chinese family with autosomal recessive muscular dystrophy-dystroglycanopathy C1.
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- Journal of Cellular & Molecular Medicine, 2017, v. 21, n. 7, p. 1388, doi. 10.1111/jcmm.13068
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- Article
A novel heterozygous COL4A4 missense mutation in a Chinese family with focal segmental glomerulosclerosis.
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- Journal of Cellular & Molecular Medicine, 2016, v. 20, n. 12, p. 2328, doi. 10.1111/jcmm.12924
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- Article
Novel Compound Heterozygous PRKN Variants in a Han-Chinese Family with Early-Onset Parkinson's Disease.
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- Parkinson's Disease (20420080), 2019, p. 1, doi. 10.1155/2019/9024894
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- Article
A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorder.
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- Molecular Medicine Reports, 2017, v. 16, n. 4, p. 4241, doi. 10.3892/mmr.2017.7053
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- Article
A Water-Soluble ESIPT Fluorescent Probe with High Quantum Yield and Red Emission for Ratiometric Detection of Inorganic and Organic Palladium.
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- Chemistry - An Asian Journal, 2015, v. 10, n. 5, p. 1142, doi. 10.1002/asia.201500114
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- Article
Clinical, radiological and pathological characteristics of moderate to fulminant psittacosis pneumonia.
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- PLoS ONE, 2022, v. 17, n. 7, p. 1, doi. 10.1371/journal.pone.0270896
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- Article
Evaluation of the efficacy of transcatheter arterial embolization combined with apatinib on rabbit VX2 liver tumors by intravoxel incoherent motion diffusion-weighted MR imaging.
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- Frontiers in Oncology, 2022, v. 12, p. 1, doi. 10.3389/fonc.2022.951587
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- Article
Identification of a novel PHEX mutation in a Chinese family with X-linked hypophosphatemic rickets using exome sequencing.
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- Biological Chemistry, 2015, v. 396, n. 1, p. 27, doi. 10.1515/hsz-2014-0187
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- Article