[Clinical and biochemical approach to mitochondrial cytopathy--pyruvate dehydrogenase complex deficiency]

Effects of Pathogen Density, Soil Moisture, and Soil pH on Biological Control of Clubroot in Chinese Cabbage by Heteroconium chaetospira.

Plant disease·2019

Control of Verticillium Yellows in Chinese Cabbage by the Dark Septate Endophytic Fungus LtVB3.

Phytopathology·2008

Structure of human holocarboxylase synthetase gene and mutation spectrum of holocarboxylase synthetase deficiency.

Human genetics·2001

A novel intronic mutation of the TAZ ( G4.5) gene in a patient with Barth syndrome: creation of a 5' splice donor site with variant GC consensus and elongation of the upstream exon.

Human genetics·2001

Chromosomal localization, structure, single-nucleotide polymorphisms, and expression of the human H-protein gene of the glycine cleavage system (GCSH), a candidate gene for nonketotic hyperglycinemia.

Journal of human genetics·2001

Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation.

Kidney international·2001

[Successful treatment with topiramate in a case of idiopathic intracranial hypertension refractory to acetazolamide].

No to hattatsu = Brain and development·2018

[Clinical characteristics of early juvenile GM2 gangliosidosis: a case report].

No to hattatsu = Brain and development·2018

[Non-invasive positive pressure ventilation during the management of severe spinal muscular atrophy type I].

No to hattatsu = Brain and development·2018

[Ictal arterial spin labeling MRI findings in two cases of acute confusional migraine].

No to hattatsu = Brain and development·2018

[A case of West syndrome with a deletion at chromosome 2q24.3-q31.3].

No to hattatsu = Brain and development·2018

[Irreversible cerebral ischemia caused by febrile status epilepticus in Sturge-Weber syndrome type III].

No to hattatsu = Brain and development·2018

Recent advances in the treatment of chronic liver diseases: focus on MASLD/MASH-related fibrosis.

Clinical and experimental hepatology·2026

Biological age acceleration and extrahepatic multimorbidity in U.S. adults with metabolic dysfunction-associated steatotic liver disease: a national cross-sectional study.

Clinical and experimental hepatology·2026

Plasma Metabolites for Identifying Bacterial Infection in Acute-on-chronic Liver Failure: A Prospective Multicenter Study.

Journal of clinical and translational hepatology·2026

Short-Chain Fatty Acids: Microbial Metabolites Driving Gut-Eye Axis Signaling.

Comprehensive physiology·2026

AI-driven diagnostic and prognostic models for metabolic dysfunction-associated steatotic liver disease: insights from clinical, imaging, and multi-omics studies-a scoping review.

Frontiers in medicine·2026

Integrative Multi-omics and Machine Learning Reveal the Therapeutic Mechanisms of Juanyu-Xiaozhi Formula in Metabolic Dysfunction-associated Steatotic Liver Disease and Hepatic Fibrosis via the AP-1/PPARγ/SCD1 Axis.

Journal of clinical and translational hepatology·2026

Related Experiment Videos

[Clinical and biochemical approach to mitochondrial cytopathy--pyruvate dehydrogenase complex deficiency]

Related Concept Videos

Effects of Pathogen Density, Soil Moisture, and Soil pH on Biological Control of Clubroot in Chinese Cabbage by Heteroconium chaetospira.

Control of Verticillium Yellows in Chinese Cabbage by the Dark Septate Endophytic Fungus LtVB3.

Structure of human holocarboxylase synthetase gene and mutation spectrum of holocarboxylase synthetase deficiency.

A novel intronic mutation of the TAZ ( G4.5) gene in a patient with Barth syndrome: creation of a 5' splice donor site with variant GC consensus and elongation of the upstream exon.

Chromosomal localization, structure, single-nucleotide polymorphisms, and expression of the human H-protein gene of the glycine cleavage system (GCSH), a candidate gene for nonketotic hyperglycinemia.

Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation.

[Successful treatment with topiramate in a case of idiopathic intracranial hypertension refractory to acetazolamide].

[Clinical characteristics of early juvenile GM2 gangliosidosis: a case report].

[Non-invasive positive pressure ventilation during the management of severe spinal muscular atrophy type I].

[Ictal arterial spin labeling MRI findings in two cases of acute confusional migraine].

[A case of West syndrome with a deletion at chromosome 2q24.3-q31.3].

[Irreversible cerebral ischemia caused by febrile status epilepticus in Sturge-Weber syndrome type III].

Recent advances in the treatment of chronic liver diseases: focus on MASLD/MASH-related fibrosis.

Biological age acceleration and extrahepatic multimorbidity in U.S. adults with metabolic dysfunction-associated steatotic liver disease: a national cross-sectional study.

Plasma Metabolites for Identifying Bacterial Infection in Acute-on-chronic Liver Failure: A Prospective Multicenter Study.

Short-Chain Fatty Acids: Microbial Metabolites Driving Gut-Eye Axis Signaling.

AI-driven diagnostic and prognostic models for metabolic dysfunction-associated steatotic liver disease: insights from clinical, imaging, and multi-omics studies-a scoping review.

Integrative Multi-omics and Machine Learning Reveal the Therapeutic Mechanisms of Juanyu-Xiaozhi Formula in Metabolic Dysfunction-associated Steatotic Liver Disease and Hepatic Fibrosis via the AP-1/PPARγ/SCD1 Axis.

Related Experiment Videos

[Clinical and biochemical approach to mitochondrial cytopathy--pyruvate dehydrogenase complex deficiency]

Related Concept Videos

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