[Acute poisoning by carbon monoxide and heating gases]

The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa.

Neurology·2008

The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V.

Neurology·2006

A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36.

Neurology·2006

'Cap myopathy': case report of a family.

Neuromuscular disorders : NMD·2006

Congenital myasthenic syndrome due to rapsyn deficiency: three cases with arthrogryposis and bulbar symptoms.

Neuropediatrics·2004

[Congenital myasthenic syndromes due to mutations in the rapsyn gene].

Revue neurologique·2004

[In utero treatment of twin-to-twin transfusion syndrome].

La Revue du praticien·2026

[In utero treatment of spina bifida].

La Revue du praticien·2026

[Syphilis and pregnancy].

La Revue du praticien·2026

[Second-line treatments for Parkinson's disease].

La Revue du praticien·2026

[Ageism in healthcare: sad prejudices!]

La Revue du praticien·2026

[Vaccination for pregnant women].

La Revue du praticien·2026

Cold atmospheric plasma affects metabolic processes in malignant melanoma.

Cancer cell international·2026

A versatile cGAMP reporter reveals principles of cGAS activation by DNA damage and chromosome instability.

Nature cell biology·2026

Cyclic Thiosulfinates: Synthesis and Applications in Chemical Biology and Materials Science.

Chembiochem : a European journal of chemical biology·2026

Rh/C-catalyzed room-temperature electrocatalytic hydrogenation of aromatic compounds in aqueous electrolyte.

Organic & biomolecular chemistry·2026

Ligand-dependent hydrogen evolution rates for (PNNP)Co catalysts.

Dalton transactions (Cambridge, England : 2003)·2026

An Unusual Presentation of Frontal Pneumosinus Dilatans as Flight-Related Headache With Favorable Response to Carbamazepine.

Cureus·2026

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[Acute poisoning by carbon monoxide and heating gases]

Related Concept Videos

The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa.

The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V.

A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36.

'Cap myopathy': case report of a family.

Congenital myasthenic syndrome due to rapsyn deficiency: three cases with arthrogryposis and bulbar symptoms.

[Congenital myasthenic syndromes due to mutations in the rapsyn gene].

[In utero treatment of twin-to-twin transfusion syndrome].

[In utero treatment of spina bifida].

[Syphilis and pregnancy].

[Second-line treatments for Parkinson's disease].

[Ageism in healthcare: sad prejudices!]

[Vaccination for pregnant women].

Cold atmospheric plasma affects metabolic processes in malignant melanoma.

A versatile cGAMP reporter reveals principles of cGAS activation by DNA damage and chromosome instability.

Cyclic Thiosulfinates: Synthesis and Applications in Chemical Biology and Materials Science.

Rh/C-catalyzed room-temperature electrocatalytic hydrogenation of aromatic compounds in aqueous electrolyte.

Ligand-dependent hydrogen evolution rates for (PNNP)Co catalysts.

An Unusual Presentation of Frontal Pneumosinus Dilatans as Flight-Related Headache With Favorable Response to Carbamazepine.

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[Acute poisoning by carbon monoxide and heating gases]

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