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You searched for: Author/Creator Sperl, Wolfgang

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1. 106 Diversity of clinical phenotype of patients with pyruvate dehydrogenase deficiency due to PDHA1 gene mutations. (11th October 2021)

2. Age-Related Deterioration of Mitochondrial Function in the Intestine. (19th August 2020)

4. Austrian study shows that delays in accessing acute paediatric health care outweighed the risks of COVID‐19. (19th August 2020)

5. Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency. Issue 1 (30th May 2015)

6. Clinical, morphological, biochemical, imaging and outcome parameters in 21 individuals with mitochondrial maintenance defect related to FBXL4 mutations. Issue 5 (14th April 2015)

7. Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies. (19th July 2017)

8. Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement. (13th March 2015)

9. Disturbed mitochondrial and peroxisomal dynamics due to loss of MFF causes Leigh-like encephalopathy, optic atrophy and peripheral neuropathy. Issue 4 (18th January 2016)

10. Erratum to: TMEM70 deficiency: long‐term outcome of 48 patients. Issue 3 (17th March 2015)