[Cardiovascular collapse in barbiturate, tranquilizing agent and phenothiazine poisoning]

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

Inflammatory pseudotumor of lymph nodes.

Annales de medecine interne·2004

[Necrolytic migratory erythema revealing glucagonoma without diabetes].

Annales de medecine interne·2004

[Bilateral primary non-Hodgkin's lymphomas of the adrenals].

Annales de medecine interne·2004

[Acute "pseudo-angiocholitis" due to colonic adenocarcinoma in a man with primary sclerosis cholangitis and ulcerative colitis].

Annales de medecine interne·2004

[Slipped capital femoral epiphysis associated with hyperparathyroidism. A case report].

Annales de medecine interne·2004

[Chronic fever revealing an urachal cyst].

Annales de medecine interne·2004

Methodological considerations for designing and conducting open-label placebo trials.

Pain·2026

Efficacy of intravenous ketamine for neuropathic pain: a systematic review and meta-analysis of randomized clinical trials.

Pain management·2026

Data-driven in silico toxicity profiling of marketed drugs and retrospective analysis of post-marketing withdrawal risk.

Toxicology mechanisms and methods·2026

Influence of sex, anxiety, and risk-taking behavior on opioid and alcohol polysubstance consumption patterns.

Addiction neuroscience·2026

Assessing the Safety of Medications During Lactation: Lactation safety.

The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG·2026

Related Experiment Videos

[Cardiovascular collapse in barbiturate, tranquilizing agent and phenothiazine poisoning]

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].

Inflammatory pseudotumor of lymph nodes.

[Necrolytic migratory erythema revealing glucagonoma without diabetes].

[Bilateral primary non-Hodgkin's lymphomas of the adrenals].

[Acute "pseudo-angiocholitis" due to colonic adenocarcinoma in a man with primary sclerosis cholangitis and ulcerative colitis].

[Slipped capital femoral epiphysis associated with hyperparathyroidism. A case report].

[Chronic fever revealing an urachal cyst].

Methodological considerations for designing and conducting open-label placebo trials.

Efficacy of intravenous ketamine for neuropathic pain: a systematic review and meta-analysis of randomized clinical trials.

Data-driven in silico toxicity profiling of marketed drugs and retrospective analysis of post-marketing withdrawal risk.

Influence of sex, anxiety, and risk-taking behavior on opioid and alcohol polysubstance consumption patterns.

Assessing the Safety of Medications During Lactation: Lactation safety.

Related Experiment Videos

[Cardiovascular collapse in barbiturate, tranquilizing agent and phenothiazine poisoning]

Related Concept Videos

Related Articles