Search Results - "Reynier, Pascal"

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An Apparently Isolated Optic Neuropathy Associated with Biallelic Variants in SLC25A46 Gene Encoding the Mitochondrial Ugo1-Like Protein.

Authors: Reynier, Pascal Amati-Bonneau, Patrizia Desquiret-Dumas, Valérie et al.

Source: Neuro-Ophthalmology. Feb2026, Vol. 50 Issue 1, p96-100. 5p.

MetabOCT: a clinical trial looking for a metabolomic signature predicting the onset of Leber's hereditary optic neuropathy in healthy MtDNA mutations carriers.

Authors: Orssaud, Christophe Reynier, Pascal

Source: Metabolomics. Oct2025, Vol. 21 Issue 5, p1-5. 5p.

Extension of Quasi-Load Insensitive Generalized Class-E Doherty Operation with Complex Load Trajectories.

Authors: Otmani, Mehdi Serhan, Ayssar Arnould, Jean-Daniel et al.

Source: Chips; Jun2025, Vol. 4 Issue 2, p26, 14p

L'embryon et ses mitochondries.

Alternate Title: Embryo and mitochondria.

Authors: May-Panloup, Pascale Reynier, Pascal

Source: Médecine de la Reproduction. jan-mar2019, Vol. 21 Issue 1, p49-58. 10p.

Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondria.

Authors: Chevrollier, Arnaud Bonnard, Adeline Alice Ruaud, Lyse et al.

Source: Brain: A Journal of Neurology; Jan2024, Vol. 147 Issue 1, p91-99, 9p

Coupled circuit/EM simulation for radio frequency circuits.

Authors: Bittner, Kai Brachtendorf, H. G. Schoenmaker, Wim et al.

Source: DAC: Annual ACM/IEEE Design Automation Conference; 2017, Issue 54, p109-114, 6p

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The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probands.

Authors: Rocatcher, Aude Desquiret-Dumas, Valérie Charif, Majida et al.

Source: Brain: A Journal of Neurology; Feb2023, Vol. 146 Issue 2, p455-460, 6p

A Novel Approach for Doherty PA Design Using a Compact L-C Combiner.

Authors: Bachi, Joe Serhan, Ayssar Pham, Dang-Kien Germain et al.

Source: IEEE Transactions on Circuits & Systems. Part II: Express Briefs; Oct2022, Vol. 69 Issue 10, p4023-4027, 5p

Is ABCC6 a genuine mitochondrial protein?

Authors: Ferré, Marc Reynier, Pascal Chevrollier, Arnaud et al.

Source: BMC Research Notes. 2013, Vol. 6 Issue 1, p1-7. 7p.

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Second report of RING finger protein 113A (RNF113A) involvement in a Mendelian disorder.

Authors: Tessarech, Marine Gorce, Magali Boussion, Françoise et al.

Source: American Journal of Medical Genetics. Part A; Mar2020, Vol. 182 Issue 3, p565-569, 5p

Updated review of postmortem biochemical exploration of hypothermia with a presentation of standard strategy of sampling and analyses.

Authors: Rousseau, Guillaume Reynier, Pascal Jousset, Nathalie et al.

Source: Clinical Chemistry & Laboratory Medicine. Nov2018, Vol. 56 Issue 11, p1819-1827. 9p. 3 Charts.

mtDNA haplogroup J: a contributing factor of optic neuritis.

Authors: Reynier, Pascal Penisson-Besnier, Isabelle Moreau, Corinne et al.

Source: European Journal of Human Genetics. Apr99, Vol. 7 Issue 3, p404. 3p.

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Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fission.

Authors: Gerber, Sylvie Charif, Majida Chevrollier, Arnaud et al.

Source: Brain: A Journal of Neurology; Oct2017, Vol. 140 Issue 10, p2586-2596, 11p

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A Nontargeted UHPLC-HRMS Metabolomics Pipeline for Metabolite Identification: Application to Cardiac Remote Ischemic Preconditioning.

Authors: Kouassi Nzoughet, Judith Bocca, Cinzia Simard, Gilles et al.

Source: Analytical Chemistry; 2/7/2017, Vol. 89 Issue 3, p2138-2146, 9p

Recurrent Isolated Neonatal Hemolytic Anemia: Think About Glutathione Synthetase Deficiency.

Authors: Signolet, Isabelle Chenouard, Rachel Oca, Florine et al.

Source: Pediatrics. Sep2016, Vol. 138 Issue 3, pe1-e5. 5p.

Subjects: Hemolytic anemia diagnosis, Enzymes, Glutathione, Hemolysis & hemolysins, Hemolytic anemia, Hyperbilirubinemia, Inborn errors of metabolism, Disease complications, Children