Lipohistiodiaresis: a syndrome of lipodystrophy universalis, accelerated growth, lipemia, hepatic cirrhosis, and insulin-resistant diabetes without ketosis.
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Child↗
Biomedical subjects
I McQUARRIE
Publications and source records attributed to I McQUARRIE.
The clinical significance of congenital deficiences of specific plasma proteins.
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Afibrinogenemia↗
Random notes concerning the etiological mechanisms and treatment of spontaneous hypoglycemia.
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Adrenocorticotropic Hormone↗
Congenital afibrinogenemia.
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Afibrinogenemia↗
Idiopathic spontaneously occurring hypoglycemia in infants; clinical significance of problem and treatment.
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Child↗
An extension of two pedigrees of hypoglycemosis.
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Heredity↗
[Study of the role of water and electrolytes in epileptic convulsions].
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Body Fluids↗
Recent studies on the role of potassium in hereditary (familial) periodic paralysis.
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Humans↗
Hereditary periodic paralysis. I. Effects of various induced changes in physiological state on paralytic attacks.
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Animals↗
Hereditary periodic paralysis. II. Effects of fasting and of various types of diet on occurrence of para lytic attacks.
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Diet↗
Observations on two children with diabetes mellitus and epilepsy.
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Child↗
Metabolic and clinical effects of corticotropin (ACTH) on essential glycogenosis (von Gierke's disease).
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Adrenocorticotropic Hormone↗
Labeled methionine as an indicator of protein formation in children with lipoid nephrosis.
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Child↗
Studies on spontaneous hypoglycemosis: the place of pituitary adrenocorticotropic hormone (ACTH) in therapy.
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Adrenocorticotropic Hormone↗
Familial hypoglycemosis of probable genetic origin.
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Blood Glucose↗
Comparison of nutritive value of mineral-enriched meat and milk.
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Animals↗
Eighty years of progress in pediatrics.
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Child↗