Creatine and coenzyme Q10 in the treatment of ALS

Assessment of bulbar function in amyotrophic lateral sclerosis: validation of a self-report scale (Center for Neurologic Study Bulbar Function Scale).

European journal of neurology·2018

Use of lumbar laminoplasty vs. laminotomy for transection of the filum terminale does not affect early complication rates or postoperative course.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery·2015

Expression and cellular localization of the classical progesterone receptor in healthy and amyotrophic lateral sclerosis affected spinal cord.

European journal of neurology·2014

Regional spread pattern predicts survival in patients with sporadic amyotrophic lateral sclerosis.

European journal of neurology·2012

Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: multidisciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Neurology·2009

Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Neurology·2009

Dementia of frontal lobe type in Kennedy's disease.

Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases·2005

Venous thrombosis in an ALS population over four years.

Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases·2005

Spirometer-dependence of vital capacity in ALS: validation of a portable device in 52 patients.

Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases·2005

A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset and incomplete penetrance in China.

Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases·2005

[SFBC/CNBH Working Group on the evaluation of blood glucose measurement in the laboratory: results of a survey conducted in France and French-speaking laboratories].

Annales de biologie clinique·2026

From urine to serum: blood-based matrices reshape the future of anti-doping testing.

Bioanalysis·2026

Prenatal urinary BTEX metabolite levels and length of gestation: preliminary results from a metropolitan Detroit birth cohort.

BMJ paediatrics open·2026

Label-free analysis of grade-specific molecular alterations in osteoarthritic subchondral bone using Raman spectroscopy coupled with MCR-ALS.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy·2026

Beyond copy number: circulating cell-free mitochondrial DNA Fragmentomics and structural states in liquid biopsy.

Clinica chimica acta; international journal of clinical chemistry·2026

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Creatine and coenzyme Q10 in the treatment of ALS

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Assessment of bulbar function in amyotrophic lateral sclerosis: validation of a self-report scale (Center for Neurologic Study Bulbar Function Scale).

Use of lumbar laminoplasty vs. laminotomy for transection of the filum terminale does not affect early complication rates or postoperative course.

Expression and cellular localization of the classical progesterone receptor in healthy and amyotrophic lateral sclerosis affected spinal cord.

Regional spread pattern predicts survival in patients with sporadic amyotrophic lateral sclerosis.

Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: multidisciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Dementia of frontal lobe type in Kennedy's disease.

Venous thrombosis in an ALS population over four years.

Spirometer-dependence of vital capacity in ALS: validation of a portable device in 52 patients.

A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset and incomplete penetrance in China.

Circulating antibodies to cysteinyl catecholamines in amyotrophic lateral sclerosis and Parkinson's disease patients.

Psychopathology in amyotrophic lateral sclerosis: a preliminary study with 27 ALS patients.

What's a White Matter 'Fiber'?

[SFBC/CNBH Working Group on the evaluation of blood glucose measurement in the laboratory: results of a survey conducted in France and French-speaking laboratories].

From urine to serum: blood-based matrices reshape the future of anti-doping testing.

Prenatal urinary BTEX metabolite levels and length of gestation: preliminary results from a metropolitan Detroit birth cohort.

Label-free analysis of grade-specific molecular alterations in osteoarthritic subchondral bone using Raman spectroscopy coupled with MCR-ALS.

Beyond copy number: circulating cell-free mitochondrial DNA Fragmentomics and structural states in liquid biopsy.

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Creatine and coenzyme Q10 in the treatment of ALS

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