Treatment options for lactic acidosis and metabolic crisis in children with mitochondrial disease

The Brain is Hypothermic in Patients with Mitochondrial Diseases

(2014) Mario Rango et al.   JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM

Genetics of mitochondrial respiratory chain deficiencies

(2014) A. Rötig   REVUE NEUROLOGIQUE

Emulsification Using Highly Hydrophilic Surfactants Improves the Absorption of Orally Administered Coenzyme Q10

(2013) Yuki Sato et al.   BIOLOGICAL & PHARMACEUTICAL BULLETIN

Sodium Bicarbonate Use in Shock and Cardiac Arrest

(2013) Melissa J. Parker et al.   CRITICAL CARE MEDICINE

Novel Mutations inSCO1as a Cause of Fatal Infantile Encephalopathy and Lactic Acidosis

(2013) Scot C. Leary et al.   HUMAN MUTATION

A guide to diagnosis and treatment of Leigh syndrome

(2013) F. Baertling et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Long-term safety of dichloroacetate in congenital lactic acidosis

(2013) Monica Abdelmalak et al.   MOLECULAR GENETICS AND METABOLISM

New treatments for mitochondrial disease—no time to drop our standards

(2013) Gerald Pfeffer et al.   Nature Reviews Neurology

Efficacy and safety of intermittent hemodialysis in infants and young children with inborn errors of metabolism

(2013) I-Jung Tsai et al.   PEDIATRIC NEPHROLOGY

Phenylbutyrate Therapy for Pyruvate Dehydrogenase Complex Deficiency and Lactic Acidosis

(2013) R. Ferriero et al.   Science Translational Medicine

Pediatric Renal Replacement Therapy in the Intensive Care Unit

(2012) Brian C. Bridges et al.   BLOOD PURIFICATION

Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases

(2012) S. Koene et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Treatment of acute metabolic acidosis: a pathophysiologic approach

(2012) Jeffrey A. Kraut et al.   Nature Reviews Nephrology

Monogenic Mitochondrial Disorders

(2012) Werner J.H. Koopman et al.   NEW ENGLAND JOURNAL OF MEDICINE

Thiamine Pyrophosphokinase Deficiency in Encephalopathic Children with Defects in the Pyruvate Oxidation Pathway

(2011) Johannes A. Mayr et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Thiamine supplementation in the critically ill

(2011) William Manzanares et al.   CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE

In Vivo Evidence for Lactate as a Neuronal Energy Source

(2011) M. T. Wyss et al.   JOURNAL OF NEUROSCIENCE

Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation

(2010) T. Honzik et al.   ARCHIVES OF DISEASE IN CHILDHOOD

Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene

(2010) Mike Gerards et al.   BRAIN

Sodium Bicarbonate Administration and Outcome in Preterm Infants

(2010) Carly S. Berg et al.   JOURNAL OF PEDIATRICS

A modern approach to the treatment of mitochondrial disease

(2009) Sumit Parikh et al.   Current Treatment Options in Neurology

Neuroprotective Role of Lactate after Cerebral Ischemia

(2009) Carole Berthet et al.   JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM

Role of dichloroacetate in the treatment of genetic mitochondrial diseases☆

(2008) Peter W. Stacpoole et al.   ADVANCED DRUG DELIVERY REVIEWS

Bicarbonate Therapy in Severe Metabolic Acidosis

(2008) S. Sabatini et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Evaluation of Long-term Treatment of Children With Congenital Lactic Acidosis With Dichloroacetate

(2008) P. W. Stacpoole et al.   PEDIATRICS

Sodium Bicarbonate: Basically Useless Therapy

(2008) J. L. Aschner et al.   PEDIATRICS

Prevalence of mitochondrial DNA disease in adults

(2007) Andrew M. Schaefer et al.   ANNALS OF NEUROLOGY