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1.
Adulteration of proprietary Chinese medicines and health products with undeclared drugs: experience of a tertiary toxicology laboratory in Hong Kong.
Br J Clin Pharmacol
; 84(1): 172-178, 2018 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-28965348
2.
Serum ceruloplasmin monitoring in a case of silver intoxication due to intravenous silver infusion.
Clin Toxicol (Phila)
; 60(2): 255-258, 2022 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-34047646
3.
Toxicity from illegitimate slimming agents - a 10-year case series at a tertiary toxicology laboratory in Hong Kong.
Clin Toxicol (Phila)
; 59(5): 426-432, 2021 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-32960101
4.
In-house multiplex ligation-dependent probe amplification assay for citrin deficiency: analytical validation and novel exonic deletions in SLC25A13.
Pathology
; 53(7): 867-874, 2021 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-34045052
5.
Urine organic acid as the first clue towards aromatic L-amino acid decarboxylase (AADC) deficiency in a high prevalence area.
Clin Chim Acta
; 521: 40-44, 2021 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-34161777
6.
Genetic diagnosis of CADASIL in three Hong Kong Chinese patients: A novel mutation within the intracellular domain of NOTCH3.
J Clin Neurosci
; 56: 95-100, 2018 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-29980472
7.
First case of genetically confirmed CLN3 disease in Chinese with cDNA sequencing revealing pathogenicity of a novel splice site variant.
Clin Chim Acta
; 486: 151-155, 2018 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-30053402
8.
Nuclear magnetic resonance spectroscopy-based urinalysis for a young girl with extreme hypoglycaemia.
Pathology
; 54(4): 505-508, 2022 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-34702582
9.
McArdle disease presenting as abnormal liver function: biochemical, anatomical and genetic characterisation in the first genetically confirmed Chinese family with a novel splicing variant.
Pathology
; 53(5): 670-673, 2021 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-33309034
10.
Urinary bladder stone due to adenine phosphoribosyltransferase deficiency: first genetically confirmed case in a Chinese patient.
Pathology
; 51(5): 557-561, 2019 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-31201003
11.
Successful Adaptation of Targeted Gene Panel Next-Generation Sequencing in Regional Hospital in Hong Kong: Genomic Diagnosis of SCN2A-Related Seizure Disorder.
Chin Med J (Engl)
; 131(18): 2262-2264, 2018 Sep 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-30203812
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