Search Results - "Lenard, H. G."
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1
Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy
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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2
Fetal CNS damage after exposure to maternal trauma during pregnancy
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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3
CT and MRI of congenital sinonasal ossifying fibroma
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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4
The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2) : compiled data from 10 pedigrees
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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5
Relapsing polychondritis in childhood: case report and short review
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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6
Paraneoplastic limbic encephalitis in two teenage girls
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
Long-term culture and characterization of human neurofibroma-derived Schwann cells
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
Motor performance and handedness in children with developmental language disorder
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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9
Aplasia cutis congenita and enlarged parietal foramina (Catlin marks) in a family
Published in Acta pædiatrica (Oslo) (01-06-1995)Get more information
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10
Clinical and genetic aspects of X-linked adrenoleukodystrophy
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
Complete remission of a diffuse pontine glioma
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
Rapid Progressive Subacute Sclerosing Panencephalitis in a 2-Year-Old Child with Congenital Athyreosis
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
Intracranial germ cell tumors: a comprehensive update of the European data
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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14
Dacrystic seizures reconsidered
Published in Neuropediatrics (01-04-1999)Get more information
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15
Spontaneous regression of a temporal arachnoid cyst
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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16
Characteristic clinical features of idiopathic neuralgic amyotrophy in childhood
Published in Neuropediatrics (01-04-2001)Get more information
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17
End-of-life decisions in neonatal intensive care: physicians' self-reported practices in seven European countries
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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18
Psychogenic contractures: the magic side of medicine
Published in Neuropediatrics (01-06-2002)Get more information
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19
Cerebral metabolic changes in biotinidase deficiency
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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20
A new leukoencephalopathy with bilateral anterior temporal lobe cysts
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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