凌子淇醫生 - 化學病理學
化學病理學專科醫生
重點資料
- 醫務委員會註冊已驗證
- 化學病理學專科醫生香港大學內外全科醫學士 · 香港病理學專科學院院士 · 2016 年醫科畢業
- 保險計劃資料整理中｜查看詳情
關於醫生
凌子淇醫生是香港註冊的化學病理學專科醫生。
學歷
保險計劃
醫院轉介
可轉介入以下私家醫院
常見問題
凌子淇醫生好嗎？
凌子淇醫生是香港註冊的化學病理學專科醫生。資歷及註冊資料來自香港醫務委員會。ok.med 不評分，也不排名。
凌子淇醫生是做什麼的？
凌子淇醫生是化學病理學醫生。
研究及論文
共 12 篇
按論文主題篩選
主題由同一批 PubMed 論文的醫學分類整理，不代表醫生提供相關診治服務。
- Meropenem interference on phosphate measurement: utility of reaction curve analysis in automated biochemistry analyzers.Clinica chimica acta; international journal of clinical chemistry · 2026
- Clavulanate contamination causes negative interference on creatinine determination by the Jaffe method but not the enzymatic method.Pathology · 2026
- A missense variant in SLC12A3 gene enhances aberrant splicing causing Gitelman syndrome.Clinica chimica acta; international journal of clinical chemistry · 2025
- Slow-Channel Congenital Myasthenic Syndrome due to a CHRNA1 Variant Masquerading as Atypical Anorexia Nervosa: A Case Report.Cureus · 2025
- Allan-Herndon-Dudley syndrome in Hong Kong: Implication for newborn screening.Clinica chimica acta; international journal of clinical chemistry · 2023
- Serum ceruloplasmin monitoring in a case of silver intoxication due to intravenous silver infusion.Clinical toxicology (Philadelphia, Pa.) · 2022
- Nuclear magnetic resonance spectroscopy-based urinalysis for a young girl with extreme hypoglycaemia.Pathology · 2022
- Urine organic acid as the first clue towards aromatic L-amino acid decarboxylase (AADC) deficiency in a high prevalence area.Clinica chimica acta; international journal of clinical chemistry · 2021
- Centrosome-associated CDC25B is a novel disease-causing gene for a syndrome with cataracts, dilated cardiomyopathy, and multiple endocrinopathies.Clinica chimica acta; international journal of clinical chemistry · 2020
- Deoxythymidylate kinase, DTYMK, is a novel gene for mitochondrial DNA depletion syndrome.Clinica chimica acta; international journal of clinical chemistry · 2019
- Clinical whole-exome sequencing reveals a common pathogenic variant in patients with CoQ<sub>10</sub> deficiency: An underdiagnosed cause of mitochondriopathy.Clinica chimica acta; international journal of clinical chemistry · 2019
- Genetic diagnosis of CADASIL in three Hong Kong Chinese patients: A novel mutation within the intracellular domain of NOTCH3.Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia · 2018
論文資料來自 PubMed／Europe PMC，按姓名及機構自動配對；每項均可按連結核對。
僅供參考，不構成醫療建議。 閱讀完整免責聲明