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Opisthotonus

Known as: Opisthotonos 
National Institutes of Health

Related topics

Related topics

14 relations
3-methylcrotonyl CoA carboxylase 1 deficiencyAdenylosuccinate lyase deficiency (disorder)COLD-INDUCED SWEATING SYNDROME 1Canavan Disease
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Broader (1)

nervous system disorder

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
The semiology of tilt-induced reflex syncope in relation to electroencephalographic changes.
Syncope is defined as transient loss of consciousness as a result of cerebral hypoperfusion. Electroencephalography during… Expand
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Review
2002
Review
2002
Seizure-like phenomena and propofol: A systematic review
Abstract—Data on seizure-like phenomena (SLP) in patients receiving propofol were systematically reviewed. Reports had to provide… Expand
Review
1998
Review
1998
Role of Propofol in Refractory Status Epilepticus
OBJECTIVE: To provide a review of the proposed mechanism of action, clinical efficacy, adverse effects, and therapeutic… Expand
Highly Cited
1997
Highly Cited
1997
Acute 3-nitropropionic acid intoxication induces striatal astrocytic cell death and dysfunction of the blood-brain barrier: involvement of dopamine toxicity
Mechanisms underlying the selective vulnerability of the lateral striatal area to the toxic effects of 3-nitropropionic acid (3… Expand
Highly Cited
1997
Highly Cited
1997
The Type 1 Inositol 1,4,5-Trisphosphate Receptor Gene Is Altered in the opisthotonos Mouse
The opisthotonos (opt) mutation arose spontaneously in a C57BL/Ks-db2J colony and is the only known, naturally occurring allele… Expand
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Highly Cited
1991
Highly Cited
1991
Novel myosin heavy chain encoded by murine dilute coat colour locus
Nature 349, 709-713 (1991) WE have discovered frameshift errors made in the assembly of our published cDNA sequence affecting… Expand
Highly Cited
1991
Highly Cited
1991
Novel myosin heavy chain encoded by murine dilute coat colour locus
HUNDREDS of murine dilute mutations have been identified and analysed, making dilute one of the best genetically characterized of… Expand
Review
1987
Review
1987
Symptomatic Arnold-Chiari malformation: review of experience with 22 cases.
Twenty-two patients with closed myelomeningoceles, shunted hydrocephalus, and symptomatic Arnold-Chiari malformations were… Expand
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Highly Cited
1983
Highly Cited
1983
Experience with surgical decompression of the Arnold-Chiari malformation in young infants with myelomeningocele.
Forty-five infants with myelomeningocele in whom hydrocephalus was absent or adequately controlled developed signs and symptoms… Expand
Highly Cited
1977
Highly Cited
1977
Withdrawal symptoms in infants with the fetal alcohol syndrome.
Six infants with dysmorphic features of the fetal alcohol syndrome presented with symptoms of withdrawal from alcohol similar to… Expand
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