Search Results - "Grunnet, M L"

An antibody to lymphotoxin and tumor necrosis factor prevents transfer of experimental allergic encephalomyelitis by RUDDLE, N. H, BERGMAN, C. M, MCGRATH, K. M, LINGENHELD, E. G, GRUNNET, M. L, PADULA, S. J, CLARK, R. B

“…Uncertainty regarding pathogenic mechanisms has been a major impediment to effective prevention and treatment for human neurologic diseases such as multiple…”
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Autosomal dominant Emery-Dreifuss dystrophy due to mutations in rod domain of the lamin A/C gene by FELICE, K. J, SCHWARTZ, R. C, BROWN, C. A, LEICHER, C. R, GRUNNET, M. L

“…Autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) is a disorder characterized clinically by humeropelvic weakness, contractures, and…”
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Adult-onset MLD : A gene mutation with isolated polyneuropathy by FELICE, K. J, GOMEZ LIRA, M, NATOWICZ, M, GRUNNET, M. L, TSONGALIS, G. J, SIMA, A. A. F, KAPLAN, R. F

“…A 22-year-old man presented with recurrent ulnar mononeuropathies and diffusely slow nerve conduction velocities. Arylsulfatase A (ASA) activity from…”
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Broad immunocytochemical localization of the formylpeptide receptor in human organs, tissues, and cells by Becker, E L, Forouhar, F A, Grunnet, M L, Boulay, F, Tardif, M, Bormann, B J, Sodja, D, Ye, R D, Woska, Jr, J R, Murphy, P M

“…The formylpeptide receptor (FPR), previously found only on polymorphonuclear leukocytes and monocytes/macrophages, responds to both synthetic N-formyl…”
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Correlation of tumor p53 and PCNA with response and survival of glioblastoma in patients treated with an ECOG protocol of pre-irradiation chemotherapy by Grunnet, M L, O'Neill, A, Gilbert, M, Hellman, R

“…The ability to predict treatment responsiveness and survival of patients with glioblastoma multiforme, the most malignant and most common primary brain tumor,…”
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A lectin and synaptophysin study of developing brain by Grunnet, M.L.

“…Lectins which bind to carbohydrate residues of glycoconjugates can be used as histochemical markers of these substances. A battery of lectins including peanut…”
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Selective atrophy of type 1 muscle fibers in McArdle's disease by FELICE, K. J, GRUNNET, M. L, SIMA, A. A. F

“…McArdle's disease is a metabolic myopathy of glycogen utilization caused by an absence or deficiency of myophosphorylase. The muscle biopsy features include…”
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Autosomal dominant centronuclear myopathy: Report of a new family with clinical features simulating facioscapulohumeral syndrome by Felice, Kevin J., Grunnet, Margaret L.

“…The centronuclear myopathies are a clinically and genetically heterogeneous group of disorders which share similar histological features on muscle biopsy. The…”
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Childhood-onset spinocerebellar syndrome associated with massive polyglucosan body deposition by Felice, K. J., Grunnet, M. L., Rao, K. R., Wolfson, L. I.

“…Introduction – Polyglucosan body disease (PBD) is a progressive neurological disorder beginning in adult life and associated pathologically with widespread…”
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Morphologic Evidence for a Preferential Storage of Tissue Plasminogen Activator (t-PA) in Perivascular Axons of the Rat Uvea by WANG, YAFEI, HAND, ARTHUR R, GILLIES, CONCETTINA, GRUNNET, MARGARET L, CONE, ROBERT E, O'ROURKE, JAMES

“…The uveal layer is thought to hold the largest stores of tissue plasminogen activator (t-PA) within the eye. However, the uveal cell types that contain and…”
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Inclusion body myositis associated with a severe unilateral levodopa-responsive upper extremity tremor by Felice, Kevin J., Grunnet, Margaret L.

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Primary lateral sclerosis in a child by GRUNNET, M. L, LEICHER, C, ZIMMERMAN, A, ZALNERAITIS, E, BARWICK, M

“…Primary lateral sclerosis (PLS), previously undescribed in children, is characterized by a spastic motor deterioration and pathologic demonstration of…”
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Polymyositis with tubular aggregates by Grunnet, M L, Abeles, M, Hofbauer, H

“…We report a patient with classic idiopathic polymyositis who had tubular aggregates on muscle biopsy. Tubular aggregates are distinctly rare in polymyositis…”
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Effects of fetal insulin secretory deficiency on metabolism in fetal lamb by Philipps, A. F., Rosenkrantz, T. S., Grunnet, M. L., Connolly, M. E., Porte, P. J., Raye, J. R.

“…Effects of fetal insulin secretory deficiency on metabolism in fetal lamb. A F Philipps , T S Rosenkrantz , M L Grunnet , M E Connolly , P J Porte and J R Raye…”
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Periventricular leukomalacia complex by Grunnet, M L

“…At autopsy in the past three years, a new complex of CNS lesions has appeared in 54% (50/93) of the brains of premature infant cadavers that have come from our…”
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Effects of fetal insulin secretory deficiency on metabolism in fetal lamb by PHILIPPS, A. F, ROSENKRANTZ, T. S, GRUNNET, M. L, CONNOLLY, M. E, PORTE, P. J, RAYE, J. R

“…Fetal insulin secretion may be of importance in determining both fetal metabolic rate and glucose homeostasis in the resting state. To investigate this…”
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The clinical course in the periventricular leukomalacia complex by Grunnet, M L, Conard, F U

“…Intraventricular hemorrhage (IVH) and classical periventricular leukomalacia complex are considered the two most common forms of perinatal anoxic-ischemic…”
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Muscle biopsy and the clinical course of infantile spinal muscular atrophy by Zalneraitis, E L, Halperin, J J, Grunnet, M L, Russman, B S, Peress, N

“…Eight infants with severe early infantile spinal muscular atrophy diagnosed by clinical presentation and muscle biopsy were studied. The extent of alterations…”
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Möbius sequence: further in vivo support for the subclavian artery supply disruption sequence by St Charles, S, DiMario, Jr, F J, Grunnet, M L

“…Möbius sequence consists of a congenital bilateral facial nerve palsy and external ophthalmoplegia often associated with malformations of the limbs and…”
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Ultrastructure and electrodiagnosis of peripheral neuropathy in Cockaynés syndrome by GRUNNET, M. L, ZIMMERMAN, A. W, LEWIS, R. A

“…Cockayne's syndrome is a multisystem disease that begins in infancy and is inherited as an autosomal recessive. We studied a 4-year-old girl with nystagmus,…”
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