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A systematic study of a panel of mitochondrial functional testing in fibroblasts shows strong clinical utility
(2021) JOURNAL OF INHERITED METABOLIC DISEASE. In Journal of inherited metabolic disease 44(S1). p.139-140 -
New mitochondrial diagnostic testing in fibroblasts, a minimally invasive tissue, identifies sensitive functional testing methods for complex I deficient primary mitochondrial disorders
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- Journal Article
- A1
- open access
GN-model validation over seven fiber types in uncompensated PM-16QAM Nyquist-WDM links
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- Journal Article
- A1
- open access
1306-km 20x124.8-Gb/s PM-64QAM transmission over PSCF with Net SEDP 11,300 (b.km)/s/Hz using 1.15 samp/symb DAC
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- Conference Paper
- C1
- open access
1306-km 20x124.8-Gb/s PM-64QAM transmission over PSCF with Net SEDP 11,300 (b km)/s/Hz using 1.15 samp/symb DAC
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- Conference Paper
- P1
- open access
Extensive fiber comparison and GN-model validation in uncompensated links using DAC-generated Nyquist-WDM PM-16QAM channels
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The Manoeuvring Committee - Final Report and Recommendations to the 23rd ITTC.
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Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2.
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The Manoeuvring Committee. Final Report and Recommendations to the 22nd ITTC
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Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.