Published in Neuropediatrics on November 01, 1981
Isolation of a major protein component of Rosenthal fibers. Am J Pathol (1988) 1.38
Alexander's disease in a Bernese mountain dog. Acta Neuropathol (1996) 0.79
MS-like presentation of Alexander disease with multifocal lesions and oligoclonal bands. J Neurol (2010) 0.78
Relation of smoking and alcohol and coffee consumption to active Helicobacter pylori infection: cross sectional study. BMJ (1997) 2.65
Cumulative incidence rates of the mucopolysaccharidoses in Germany. J Inherit Metab Dis (2005) 2.40
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy. Nat Genet (1999) 2.04
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes. Ann Neurol (1999) 2.02
Parental smoking and infection with Helicobacter pylori among preschool children in southern Germany. Epidemiology (1998) 1.98
Helicobacter pylori among preschool children and their parents: evidence of parent-child transmission. J Infect Dis (1999) 1.96
Desmin myopathy. Brain (2004) 1.79
Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions. Am J Hum Genet (1987) 1.72
Demonstration of a phospholipid-rich zone in the human gastric epithelium damaged by Helicobacter pylori. Gastroenterology (1993) 1.66
Stimulation of leukocyte/endothelium interaction by oxidized low-density lipoprotein in hairless mice. Involvement of CD11b/CD18 adhesion receptor complex. Lab Invest (1993) 1.64
Acquisition of Helicobacter pylori infection in a high-risk population occurs within the first 2 years of life. J Pediatr (2000) 1.53
Characteristic distribution pattern of Helicobacter pylori in dental plaque and saliva detected with nested PCR. J Med Microbiol (2000) 1.50
Alcohol consumption and Helicobacter pylori infection: results from the German National Health and Nutrition Survey. Epidemiology (1999) 1.45
Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy. Proc Natl Acad Sci U S A (1996) 1.44
Helicobacter pylori infection among offspring of patients with stomach cancer. Gastroenterology (2000) 1.42
Coronary heart disease risk reduction in a predominantly beer-drinking population. Epidemiology (2001) 1.40
Coccoid like forms (CLF) of Helicobacter pylori. Enzyme activity and antigenicity. Zentralbl Bakteriol (1993) 1.38
[Lipomucopolysaccharidosis, A new storage disease]. Z Kinderheilkd (1968) 1.38
Cytokine expression profile in idiopathic inflammatory myopathies. J Neuropathol Exp Neurol (1996) 1.34
Ultrastructure of human and experimental ependymomas. A comparative study. J Neuropathol Exp Neurol (1972) 1.31
Inverse relationship between gastric colonization of Helicobacter pylori and diarrheal illnesses in children: results of a population-based cross-sectional study. J Infect Dis (2000) 1.29
Ultrastructural localisation of urease in outer membrane and periplasm of Campylobacter pylori. J Clin Pathol (1989) 1.29
Hearing loss in facioscapulohumeral dystrophy. Eur J Pediatr (1986) 1.28
Neuromyopathy and vitamin E deficiency in man. Neuropediatrics (1981) 1.26
Familial epilepsy and yellow teeth--a disease of the CNS associated with enamel hypoplasia. Helv Paediatr Acta (1974) 1.26
Current infection with Helicobacter pylori, but not seropositivity to Chlamydia pneumoniae or cytomegalovirus, is associated with an atherogenic, modified lipid profile. Arterioscler Thromb Vasc Biol (2001) 1.22
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies). Neuromuscul Disord (2000) 1.22
Beneficial effects of alpha-lipoic acid and ascorbic acid on endothelium-dependent, nitric oxide-mediated vasodilation in diabetic patients: relation to parameters of oxidative stress. Free Radic Biol Med (2001) 1.21
Consequences of mutations within the C terminus of the FHL1 gene. Neurology (2009) 1.18
Early lesion of Pelizaeus-Merzbacher disease: electron microscopic and biochemical study. J Neuropathol Exp Neurol (1973) 1.13
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder. Acta Neuropathol (1987) 1.13
Leukodystrophy incidence in Germany. Am J Med Genet (1997) 1.12
Myopathy associated with Marfan's syndrome. Fine structural and histochemical observations. Neurology (1973) 1.12
Structural, functional and mutational analysis of the pfr gene encoding a ferritin from Helicobacter pylori. Microbiology (1998) 1.11
Tumor-like amyloid formation (amyloidoma) in the brain. J Neurol (1981) 1.10
Eccrine sweat glands are not innervated in hereditary sensory neuropathy type IV. An electron-microscopic study. Acta Neuropathol (1981) 1.10
Inclusion body myositis presenting with isolated erector spinae paresis. Neurology (1995) 1.10
Alcohol-related acute axonal polyneuropathy: a differential diagnosis of Guillain-Barré syndrome. Arch Neurol (1998) 1.10
[Herpes simplex causing a therapy-resistant panaritium (author's transl)]. Dtsch Med Wochenschr (1977) 1.09
Prevalence and determinants of Helicobacter pylori infection in preschool children: a population-based study from Germany. Int J Epidemiol (1998) 1.09
Mucolipidosis IV: novel mutation and diverse ultrastructural spectrum in the skin. Neuropediatrics (2002) 1.09
A mutation in myotilin causes spheroid body myopathy. Neurology (2005) 1.07
Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy. Neurology (2003) 1.07
Significance of muscle biopsies in neuronal ceroid-lipofuscinoses. J Neurol Neurosurg Psychiatry (1975) 1.07
Lesions of the pontine tegmentum and conjugate gaze paralysis. Arch Neurol (1971) 1.06
Compressed air injury of the orbit in the absence of external trauma. Eye (Lond) (2003) 1.04
Impaired discrimination between stereoisomers of alpha-tocopherol in patients with familial isolated vitamin E deficiency. J Lipid Res (1993) 1.04
Hyperphosphatasia with mental retardation. J Pediatr (1988) 1.04
Helicobacter pylori in dental plaque: a comparison of different PCR primer sets. Dig Dis Sci (1999) 1.04
Mallory body-like inclusions in a hereditary congenital neuromuscular disease. Muscle Nerve (1983) 1.04
Confirmation of virtual unmyelinated fiber absence in hereditary sensory neuropathy type IV. J Neuropathol Exp Neurol (1980) 1.03
The cytoplasmic bodies in a congenital myopathy can be stained with antibodies to desmin, the muscle-specific intermediate filament protein. Acta Neuropathol (1983) 1.03
Identification and characterization of an ATPase system of Helicobacter pylori and the effect of proton pump inhibitors. Am J Gastroenterol (1993) 1.03
On the ultrastructural diversity and essence of residual bodies in neuronal ceroid-lipofuscinosis. Mech Ageing Dev (1979) 1.02
Invasion of campylobacter-like organisms in the duodenal mucosa in patients with active duodenal ulcer. Klin Wochenschr (1987) 1.02
An ultrastructural study of the retina in the Jansky-Bielschowsky type of neuronal ceroid-lipofuscinosis. Am J Ophthalmol (1977) 0.99
Rigid spine syndrome in a girl. J Neurol (1982) 0.99
Human ontogenesis. 3. Cell death in fetal muscle. Acta Neuropathol (1991) 0.99
In vitro inhibition of Helicobacter pylori urease: biochemical and ultrastructural analysis. Eur J Clin Invest (1991) 0.99
Desmin splice variants causing cardiac and skeletal myopathy. J Med Genet (2000) 0.99
Prenatal diagnosis of carbamoyl phosphate synthetase I deficiency by identification of a missense mutation in CPS1. Hum Mutat (1998) 0.99
[Rhegmatogenous retinal detachment in atrophia gyrata: pars plana vitrectomy with silicone oil instillation]. Klin Monbl Augenheilkd (1996) 0.98
Congenital myopathies--a comprehensive update of recent advancements. Acta Neurol Scand (2009) 0.98
Studies on GM1-gangliosidosis, type II. Acta Neuropathol (1974) 0.98
A case of lipogranulomatosis Farber: some clinical and ultrastructural aspects. Eur J Pediatr (1985) 0.97
Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscle. J Neurol Sci (2003) 0.97
Human forms of neuronal ceroid-lipofuscinosis (Batten disease): consensus on diagnostic criteria, Hamburg 1992. J Inherit Metab Dis (1993) 0.96
Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosis. Neuropediatrics (1988) 0.96
Incidence of neuronal ceroid-lipofuscinoses in West Germany: variation of a method for studying autosomal recessive disorders. Am J Med Genet (1992) 0.96
Dystrophin as a diagnostic marker in Duchenne and Becker muscular dystrophy. Correlation of immunofluorescence and western blot. Neuropediatrics (1991) 0.96
Treatment of gustatory hyperlacrimation (crocodile tears) with injection of botulinum toxin into the lacrimal gland. Eye (Lond) (2002) 0.96
Increased ammonia production during forearm ischemic work test in McArdle's disease. Klin Wochenschr (1981) 0.96
Role of leukotrienes in leukocyte adhesion following systemic administration of oxidatively modified human low density lipoprotein in hamsters. J Clin Invest (1991) 0.96
Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndrome. Am J Med Genet (1998) 0.95
Acute infantile spinal muscular atrophy. Muscle apoptosis as a proposed pathogenetic mechanism. Brain (1990) 0.95
Fibre type disproportion in the rigid spine syndrome. Neuropadiatrie (1977) 0.95
CLN5 mutations are frequent in juvenile and late-onset non-Finnish patients with NCL. Neurology (2010) 0.95
Hyperammonaemic encephalopathy after initiation of valproate therapy in unrecognised ornithine transcarbamylase deficiency. J Neurol Neurosurg Psychiatry (1998) 0.95
Peripheral motor and sensory neuropathy of early childhood, simulating Werdnig-Hoffmann disease. Neuropadiatrie (1976) 0.95
Diagnostic immunohistochemistry in neuromuscular disorders. Histopathology (2005) 0.94
Helicobacter pylori infection and serum ferritin: A population-based study among 1806 adults in Germany. Am J Gastroenterol (2001) 0.94
Dementia in the neuronal ceroid-lipofuscinoses. Adv Exp Med Biol (2001) 0.94
Properties and function of the P type ion pumps cloned from Helicobacter pylori. Acta Physiol Scand Suppl (1998) 0.93
DNA-fragmentation and expression of apoptosis-related proteins in muscular dystrophies. Neuropathol Appl Neurobiol (1997) 0.93
Identification and characterization of Helicobacter pylori phospholipase C activity. Zentralbl Bakteriol (1993) 0.93
Juvenile Huntington chorea: clinical, ultrastructural, and biochemical studies. Neurology (1978) 0.93
Morphologic studies on adult neuronal-ceroid lipofuscinosis (NCL). Clin Neuropathol (1982) 0.93
Macrophages in multiple sclerosis. Immunobiology (1996) 0.92
DNA-fragmentation and expression of apoptosis-related proteins in experimentally denervated and reinnervated rat facial muscle. Neuropathol Appl Neurobiol (1997) 0.92
Apoptosis-related proteins in skeletal muscle fibers of spinal muscular atrophy. J Neuropathol Exp Neurol (1997) 0.92
Retinal ultrastructure of neuronal ceroid-lipofuscinosis in the dalmatian dog. Acta Neuropathol (1985) 0.92
Pigmentoarchitectonic pathology of the isocortex in juvenile neuronal ceroid-lipofuscinosis: axonal enlargements in layer IIIab and cell loss in layer V. Acta Neuropathol (1979) 0.92
Congenital myopathy with cytoplasmic bodies. Neuropediatrics (1981) 0.92
The ultrastructural variability of non-specific lipopigments. Acta Neuropathol (1979) 0.92
Antioxidant and prooxidant activity of alpha-tocopherol in human plasma and low density lipoprotein. J Lipid Res (1996) 0.91
Impaired plasma antioxidative defense and increased nontransferrin-bound iron during high-dose chemotherapy and radiochemotherapy preceding bone marrow transplantation. Free Radic Biol Med (2000) 0.91
Plasma ubiquinol-10 is decreased in patients with hyperlipidaemia. Atherosclerosis (1997) 0.91