Search Results - "Hartlage, P L"

Seizures associated with stroke in childhood by Yang, Jae S., Park, Yong D., Hartlage, Patricia L.

“…Seventy-three consecutive children younger than 17 years of age seen from 1978 to 1992 with acute hemiplegia from stroke, were retrospectively reviewed to…”
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Episodic spontaneous hypothermia with hyperhidrosis: implications for pathogenesis by Sheth, R D, Barron, T F, Hartlage, P L

“…Unprovoked hypothermia is an unusual presenting sign. When occurring with diaphoresis it has been referred to as episodic spontaneous hypothermia with…”
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MR imaging of moyamoya in neurofibromatosis by BROOKS, B. S, EL GAMMAL, T, ADAMS, R. J, HARTLAGE, P. L, SMITH, W. B

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Muscle imaging in neuromuscular disease using computerized real-time sonography by Fischer, A Q, Carpenter, D W, Hartlage, P L, Carroll, J E, Stephens, S

“…The results of a study utilizing computerized real-time sonography (CRS) to image muscles in patients with neuromuscular disease are presented for 67 patients,…”
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Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria) by Hommes, F A, Roesel, R A, Metoki, K, Hartlage, P L, Dyken, P R

“…A patient with the hyperornithinemia, hyperammonemia, homocitrullinuria syndrome is described. This patient represents the 12th documented case of this rare,…”
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Prenatal diagnosis of metachromatic leukodystrophy in a family with pseudo arylsulfatase A deficiency by the cerebroside sulfate loading test by Kihara, H, Ho, C K, Fluharty, A L, Tsay, K K, Hartlage, P L

“…Prenatal diagnosis was requested by a family at risk for metachromatic leukodystrophy (MLD). An examination of the family leukocyte arylsulfatase A profile…”
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Anticonvulsive drugs and blood levels of lactate, pyruvate, and glucose in children with seizures by CARTER, A. L, HARTLAGE, P. L, ELLER, A. G, HOMMES, F. A

“…Lactate, pyruvate, and glucose were determined in groups of 10 patients, each receiving single drug therapy for their seizure disorder with either phenytoin,…”
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A lesson in humanism: one doctor's experience by Hartlage, P L

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Serum carnosinase deficiency: Decreased affinity of the enzyme for the substrate by Hartlage, P. L., Roesel, R. A., Eller, A. G., Hommes, F. A.

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Internalized capillaries in hypokalemic periodic paralysis by Hartlage, P L, Soudmand, R

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Fatal infantile form of muscle phosphorylase deficiency by DiMauro, S, Hartlage, P L

“…A girl had generalized, rapidly progressive weakness beginning at age 4 weeks, and causing severe respiratory insufficiency and death at age 13 weeks…”
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Serum carnosinase deficiency: a non-disabling phenotype? by Cohen, M, Hartlage, P L, Krawiecki, N, Roesel, R A, Carter, A L, Hommes, F A

“…Serum carnosinase deficiency (McKusick 21220) is a rare condition, described in 13 cases. Ten additional individuals with serum carnosinase deficiency have…”
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Giant axonal neuropathy in a child with insulin-dependent diabetes mellitus by Hoffman, W H, Carroll, J E, Perry, G Y, Hartlage, P L, Kaminer, S J, Flowers, N C, Oh, S J, Kelly, D R

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Decreased muscle enoyl-CoA hydratase activities in patients with exercise intolerance by Carroll, J E, McGuire, B S, Hartlage, P L, Howard, J C

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Phosphorylase isoenzymes in normal and myophosphorylase-deficient human heart by Miranda, A F, Nette, E G, Hartlage, P L, DiMauro, S

“…Phosphorylase isoenzymes were studied by acrylamide-slab electrophoresis in normal tissues and in the heart of a child with a fatal infantile form of…”
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Argininosuccinic aciduria: perinatal diagnosis and early dietary management by Hartlage, P L, Coryell, M E, Hall, W K, Hahn, D A

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Electrocardiographic abnormalities in pediatric neuromuscular disease: a review by Arensman, F W, Hartlage, P L, Strong, W B

“…Cardiac abnormalities, often heralded by electrocardiographic alterations, at times may become a serious problem in patients with neuromuscular disorders and…”
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Urinary sialic acid screening in neurologic disorders by Carroll, J E, Roesel, R A, DuRant, R H, Nelson, A M, Hartlage, P L, Hahn, D A, Hommes, F A

“…Urine sialic acid was measured in 246 patients evaluated for possible neurodegenerative disorders. Total, free, and bound sialic acid excretion declined…”
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MR imaging of moyamoya in neurofibromatosis by Brooks, B S, el Gammal, T, Adams, R J, Hartlage, P L, Smith, W B

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