What's your diagnosis? Lethargy and hind limb paralysis in a day-23 timed pregnant rat.
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Animals↗
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Results for “Lethargy”
Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.
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Neonatal transport: a 3-day-old neonate with hypothermia, respiratory distress, lethargy and poor feeding.
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Ammonia↗
Intussusception presenting as profound lethargy.
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Child↗
Clinicopathologic conference no. 117. Hiccups, lung lesions, oral ulcers, and lethargy.
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Aged↗
Clinicopathologic conference: Hypothermia and lethargy.
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Alcoholism↗
Lethargy, anxiety, and impotence in a diabetic.
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Adult↗
Lethargy and confusion after total nephrectomy.
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Adult↗
An old patient with end stage renal disease and sudden onset of confusion and lethargy.
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Aged, 80 and over↗
Dealing with feelings: coping with lethargy.
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Behavior Therapy↗
Infant with lethargy, failure to thrive, and abnormal blood smear.
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Failure to Thrive↗
Lethargy and vomiting in an infant.
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Colonic Diseases↗
Headache, increasing lethargy, and left-side weakness.
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Adolescent↗
An 8-day-old male infant with poor feeding, lethargy, and an elevated anion gap metabolic acidosis.
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Acidosis↗
Lethargy from an unsuspected culprit.
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2-Propanol↗
A 24-day old with episodic lethargy, hypotonia, and apnea: the eyes have it.
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Adrenergic alpha-Agonists↗
Lethargy of laser oscillations and supermodes in free-electron lasers. I.
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Journal Article↗
Lethargy of laser oscillations and supermodes in free-electron lasers. II. Quantitative analysis.
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Journal Article↗
Partial ornithine transcarbamylase deficiency associated with recurrent hyperammonemia, lethargy and depressed sensorium.
A 6-year-old boy presented with recurrent coma associated with hyperammonemia and infection is reported. A liver biopsy revealed decreased ornithine transcarbamylase (OTC) activity (16% of normal). The enzymatic abnormality in the child is supported by the finding of elevated orotic acid excretion in his mother following a protein load, compatible with an X-linked pattern of inheritance. Since initiation of a dietary arginine supplement, the child has not had recurrent episodes of hyperammonemia.
Amino Acid Metabolism, Inborn Errors↗