[The debate of Miraxid: preparations in demand without side-effects]

Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment.

Journal of inherited metabolic disease·2015

Ophthalmological findings in children and young adults with genetically verified mitochondrial disease.

The British journal of ophthalmology·2010

Progressive encephalopathy and complex I deficiency associated with mutations in MTND1.

Neuropediatrics·2008

Deficiency of mitochondrial ATP synthase of nuclear genetic origin.

Neuromuscular disorders : NMD·2006

Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNA(phe) gene.

Neuromuscular disorders : NMD·2006

Two new mutations in the MTATP6 gene associated with Leigh syndrome.

Neuropediatrics·2005

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

Lakartidningen·2026

[Postoperative atrial fibrillation after open heart surgery].

Lakartidningen·2026

[Interaction between psychotic patients and AI-driven chatbots].

Lakartidningen·2026

[Superficial venous thrombosis of the lower extremities].

Lakartidningen·2026

[Switch from STEMI to OMI].

Lakartidningen·2026

[Maxillomandibular advancement].

Lakartidningen·2026

Draft genome sequence of Aeromonas veronii strain Naf-IIUM T8S isolated from diseased Pangasianodon hypophthalmus in Malaysia.

Microbiology resource announcements·2026

Association of Clinical Measures and Characteristics of Microbial Keratitis with Patient-Reported Visual Function.

Cornea·2026

Quantification of microglial dynamic motility in vivo.

Biotechnic & histochemistry : official publication of the Biological Stain Commission·2026

The lncRNA GAS5 Is Associated with Altered Exosomal MiR-651-5p Cargo in Microglia and May Serve as a Potential Marker of Relapsing-Remitting Multiple Sclerosis.

MicroRNA (Shariqah, United Arab Emirates)·2026

Methodological Alignment and Interpretive Boundaries in mRNA Vaccine Analysis.

Journal of evaluation in clinical practice·2026

Mild encephalitis/encephalopathy with a reversible splenial lesion (MERS): A case report and review of the literature.

Radiology case reports·2026

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Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment.

Ophthalmological findings in children and young adults with genetically verified mitochondrial disease.

Progressive encephalopathy and complex I deficiency associated with mutations in MTND1.

Deficiency of mitochondrial ATP synthase of nuclear genetic origin.

Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNA(phe) gene.

Two new mutations in the MTATP6 gene associated with Leigh syndrome.

[The Swedish Neonatal Quality Register (SNQ) - a complete register for a complex chain of events].

[Postoperative atrial fibrillation after open heart surgery].

[Interaction between psychotic patients and AI-driven chatbots].

[Superficial venous thrombosis of the lower extremities].

[Switch from STEMI to OMI].

[Maxillomandibular advancement].

Draft genome sequence of Aeromonas veronii strain Naf-IIUM T8S isolated from diseased Pangasianodon hypophthalmus in Malaysia.

Association of Clinical Measures and Characteristics of Microbial Keratitis with Patient-Reported Visual Function.

Quantification of microglial dynamic motility in vivo.

The lncRNA GAS5 Is Associated with Altered Exosomal MiR-651-5p Cargo in Microglia and May Serve as a Potential Marker of Relapsing-Remitting Multiple Sclerosis.

Methodological Alignment and Interpretive Boundaries in mRNA Vaccine Analysis.

Mild encephalitis/encephalopathy with a reversible splenial lesion (MERS): A case report and review of the literature.

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