Search Results - "Lenard, H. G."

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  1. 1

    Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy by HERRMANN, Ralf, STRAUB, Volker, BLANK, Martina, KUTZICK, Christian, FRANKE, Nicola, JACOB, Eva Neuen, LENARD, Hans-Gerd, KRÖGER, Stephan, VOIT, Thomas

    Published in Human molecular genetics (22-09-2000)
    “…Limb girdle muscular dystrophy is a group of clinically and genetically heterogeneous disorders inherited in an autosomal recessive or dominant mode…”
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    Fetal CNS damage after exposure to maternal trauma during pregnancy by Baethmann, M, Kahn, T, Lenard, H G, Voit, T

    Published in Acta pædiatrica (Oslo) (01-11-1996)
    “…Nine case reports are presented to indicate the possible effects of maternal trauma on surviving fetuses. Previous reports have only addressed fatal…”
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    CT and MRI of congenital sinonasal ossifying fibroma by ENGELBRECHT, V, PREIS, S, HASSLER, W, LENARD, H. G

    Published in Neuroradiology (01-07-1999)
    “…We report a 9-year-old boy with a sinonasal ossifying fibroma, probably congenital, with atypical findings on CT and MRI. CT revealed a soft-tissue density…”
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    The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2) : compiled data from 10 pedigrees by BARTH, P. G, BLENNOW, G, LENARD, H.-G, BEGEER, J. H, VAN DER KLEY, J. M, HANEFELD, F, PETERS, A. C. B, VALK, J

    Published in Neurology (01-02-1995)
    “…The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, severely impaired mental and motor development, and extrapyramidal dyskinesia is…”
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    Relapsing polychondritis in childhood: case report and short review by KNIPP, S, BIER, H, HORNEFF, G, SPECKER, C, SCHUSTER, A, SCHROTEN, H, LENARD, H.-G, NIEHUES, T

    Published in Rheumatology international (2000)
    “…Relapsing polychondritis (RP) is a disease of unknown etiology and it is characterized by inflammation of the cartilage. While the clinical picture of RP in…”
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    Paraneoplastic limbic encephalitis in two teenage girls by Rosenbaum, T, Gärtner, J, Körholz, D, Janssen, G, Schneider, D, Engelbrecht, V, Göbel, U, Lenard, H G

    Published in Neuropediatrics (01-06-1998)
    “…Paraneoplastic neurological disorders represent remote effects of cancer without invasion of tumor cells into the nervous system. Limbic encephalitis is a…”
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  7. 7

    Long-term culture and characterization of human neurofibroma-derived Schwann cells by Rosenbaum, Thorsten, Rosenbaum, Claudia, Winner, Ursula, Müller, Hans Werner, Lenard, Hans-Gerd, Hanemann, C. Oliver

    Published in Journal of neuroscience research (01-09-2000)
    “…Neurofibromas are benign tumors arising from the peripheral nerve sheath and are a typical finding in neurofibromatosis type 1 (NF1). Schwann cells are the…”
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  8. 8

    Motor performance and handedness in children with developmental language disorder by Preis, S, Schittler, P, Lenard, H G

    Published in Neuropediatrics (01-12-1997)
    “…Developmental language disorder (DLD) is diagnosed when there is a failure of normal language development in a child with normal nonverbal intelligence. The…”
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    Clinical and genetic aspects of X-linked adrenoleukodystrophy by Gärtner, J, Braun, A, Holzinger, A, Roerig, P, Lenard, H G, Roscher, A A

    Published in Neuropediatrics (01-02-1998)
    “…X-linked adrenoleukodystrophy (ALD), a leukodystrophy characterized by abnormal accumulation of saturated very long chain fatty acids in brain white matter and…”
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  11. 11

    Complete remission of a diffuse pontine glioma by Lenard, H G, Engelbrecht, V, Janssen, G, Wechsler, W, Tautz, C

    Published in Neuropediatrics (01-12-1998)
    “…A patient is described in whom a large diffuse glioma of the pons extending into the midbrain was diagnosed at the age of 2 years. Biopsy showed a fibrillary…”
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  12. 12

    Rapid Progressive Subacute Sclerosing Panencephalitis in a 2-Year-Old Child with Congenital Athyreosis by Lackmann, Gerd M., Hannen, Martin, Madjlessi, Faramarz, Lenard, Hans G., Schroten, Horst

    Published in Clinical infectious diseases (01-07-2000)
    “…We present the unique case of a 2-year-old girl with congenital athyreosis who acquired primary measles virus infection at the age of 18 months, coincidentally…”
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  13. 13

    Intracranial germ cell tumors: a comprehensive update of the European data by Calaminus, G, Bamberg, M, Baranzelli, M C, Benoit, Y, di Montezemolo, L C, Fossati-Bellani, F, Jürgens, H, Kühl, H J, Lenard, H G, Curto, M L

    Published in Neuropediatrics (01-02-1994)
    “…Intracranial germ cell tumors are rare tumor entities in childhood and adolescents. Extra- and intracranial germ cell tumors are identical in their histologic…”
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    Spontaneous regression of a temporal arachnoid cyst by WEBER, R, VOIT, T, LUMENTA, C, LENARD, H.-G

    Published in Child's nervous system (01-11-1991)
    “…Surgery is considered to be the standard therapy for arachnoid cysts (ACs). We report the case of a 13-year-old boy in whom a right temporal AC disappeared…”
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    End-of-life decisions in neonatal intensive care: physicians' self-reported practices in seven European countries by Cuttini, M, Nadai, M, Kaminski, M, Hansen, G, de Leeuw, R, Lenoir, S, Persson, J, Rebagliato, M, Reid, M, de Vonderweid, U, Lenard, HG, Orzalesi, M, Saracci, R

    Published in The Lancet (British edition) (17-06-2000)
    “…The ethical issue of foregoing life-sustaining treatment for newborn infants at high risk of death or severe disability is extensively debated, but there is…”
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    Cerebral metabolic changes in biotinidase deficiency by Schürmann, M., Engelbrecht, V., Lohmeier, K., Lenard, H. G., Wendel, U., Gärtner, J.

    Published in Journal of inherited metabolic disease (01-11-1997)
    “…Clinical and metabolic changes in the central nervous system are described in a patient with biotinidase deficiency before and after biotin treatment. Lactate,…”
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    A new leukoencephalopathy with bilateral anterior temporal lobe cysts by Olivier, M, Lenard, H G, Aksu, F, Gärtner, J

    Published in Neuropediatrics (01-10-1998)
    “…We describe an identical syndrome of cystic leukoencephalopathy in three Turkish children, including two siblings. The neurological findings were noted within…”
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