Arg339Gln Is a Recurrent Variant in Rare Combined Oxidative Phosphorylation Deficiency 4: A New Patient with Biallelic <i>TUFM</i> Gene Variant. [PDF]
Mol SyndromolTekmenuray-Unal A +3 more
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Update on ADHD genetics: A practitioner's perspective: Mise à jour sur la génétique du TDAH : le point de vue d'un praticien. [PDF]
Can J PsychiatrySchachar R +3 more
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A brief history of the human liver peroxisome. [PDF]
Histochem Cell BiolDe Craemer D +2 more
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Functional connectivity patterns of the cerebellar components of intrinsic connectivity networks in clinically diagnosed probable Alzheimer's disease. [PDF]
BMC Med ImagingHari E +5 more
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Elucidating molecular pathogenesis and developing targeted therapeutic interventions for cerebrovascular endothelial cell-mediated vascular dementia. [PDF]
Front Aging NeurosciYang Y +5 more
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Encephalitis-like presentation of methylmalonic acidemia with homocystinuria in a postpartum woman: a case report. [PDF]
Front PsychiatryWang Q, Ji Z, Wang Y, Qi Z.
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Treatment of neonatal seizures: from guidelines to precision therapy. [PDF]
Mol Cell PediatrFalsaperla R, Saporito MAN, Scalia B.
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Association of FeNO Decline Rate with Symptom Improvement in COPD: A Real-World Observational Study. [PDF]
Int J Chron Obstruct Pulmon DisLi B +5 more
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Cognitive and behavioral disturbances in PSP and MSA: clinical features and imaging correlates. [PDF]
J Neural Transm (Vienna)Ruiz-Barrio I +4 more
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Incident Cardiometabolic Comorbidities in Smokers with/Without Chronic Obstructive Pulmonary Disease: A Long-Term Cohort Study. [PDF]
J Clin MedHerrero-Cortina B +7 more
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