Published in J Neurol Sci on January 15, 1999
[Ocular myasthenia gravis]. Ophthalmologe (2013) 2.00
Cerebrovascular reactivity is impaired in patients with cardiac failure. Eur Heart J (2000) 1.98
A selective defect of cytochrome c oxidase is present in brain of Alzheimer disease patients. Neurobiol Aging (2000) 1.78
MELAS associated with mutations in the POLG1 gene. Neurology (2007) 1.77
Oscillating perfusion of cell suspensions through three-dimensional scaffolds enhances cell seeding efficiency and uniformity. Biotechnol Bioeng (2003) 1.69
Functional motor compensation in amyotrophic lateral sclerosis. J Neurol (2005) 1.67
Quantitative analysis of gene expression in human articular cartilage from normal and osteoarthritic joints. Osteoarthritis Cartilage (2001) 1.63
Cathepsin D links TNF-induced acid sphingomyelinase to Bid-mediated caspase-9 and -3 activation. Cell Death Differ (2004) 1.59
Comparison of primary angioplasty with conservative therapy in patients with acute myocardial infarction and contraindications for thrombolytic therapy. Maximal Individual Therapy in Acute Myocardial Infarction (MITRA) Study Group. Catheter Cardiovasc Interv (1999) 1.39
[The effect of a lower stimulation frequency on the AV synchronicity of VDD pacemakers]. Dtsch Med Wochenschr (1997) 1.38
Prehospital resuscitation--outcome in an urban area. Eur J Emerg Med (1995) 1.38
High dose vitamin E therapy in amyotrophic lateral sclerosis as add-on therapy to riluzole: results of a placebo-controlled double-blind study. J Neural Transm (Vienna) (2004) 1.26
Uniform tissues engineered by seeding and culturing cells in 3D scaffolds under perfusion at defined oxygen tensions. Biorheology (2006) 1.24
Use of complementary and alternative medicine in patients suffering from primary headache disorders. Cephalalgia (2009) 1.21
Evidence for a mitochondrial oxidative phosphorylation defect in brains from patients with schizophrenia. Schizophr Res (2001) 1.14
Testicular dysfunction in adrenomyeloneuropathy. Eur J Endocrinol (1997) 1.11
Regulatory properties of a mutant carnitine palmitoyltransferase in human skeletal muscle. Eur J Biochem (1985) 1.11
Towards an intraoperative engineering of osteogenic and vasculogenic grafts from the stromal vascular fraction of human adipose tissue. Eur Cell Mater (2010) 1.10
Puusepp's sign--clinical significance of a forgotten pyramidal sign. Clin Neurol Neurosurg (2009) 1.06
Subtle cognitive dysfunction in adult onset myotonic dystrophy type 1 (DM1) and type 2 (DM2). Neurology (2006) 1.04
Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicism. Neurology (2005) 1.02
Different sensitivity of rabbit heart and skeletal muscle to endotoxin-induced impairment of mitochondrial function. Eur J Biochem (2001) 1.02
Recurrent orbital myositis: report of a familial incidence. Arch Neurol (1999) 1.01
External ophthalmoplegia due to ocular myositis in a patient with ophthalmic herpes zoster. Neuromuscul Disord (2004) 1.01
Studies on the immune status of children with acute lymphocytic leukaemia. I. Early phase before and after first remission. Clin Exp Immunol (1976) 0.99
Engineered cartilage generated by nasal chondrocytes is responsive to physical forces resembling joint loading. Arthritis Rheum (2008) 0.99
C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis. J Neurol (2012) 0.98
The forgotten condyle: Delayed hypoglossal nerve palsy caused by fracture of the occipital condyle. Clin Neurol Neurosurg (1998) 0.98
Endocrine abnormalities in mitochondrial myopathy with external ophthalmoplegia. Clin Investig (1992) 0.97
Cardiac involvement in limb-girdle muscular dystrophy 2I : conventional cardiac diagnostic and cardiovascular magnetic resonance. J Neurol (2006) 0.97
Differential cartilaginous tissue formation by human synovial membrane, fat pad, meniscus cells and articular chondrocytes. Osteoarthritis Cartilage (2006) 0.96
Structural characterization and reliable biomechanical assessment of integrative cartilage repair. J Biomech (2005) 0.95
Images in clinical medicine. Retroperitoneal hemorrhage. N Engl J Med (2001) 0.95
Impaired energy metabolism in hearts of septic baboons: diminished activities of Complex I and Complex II of the mitochondrial respiratory chain. Shock (1999) 0.94
[Muscular dystrophy due to mutations in anoctamin 5: clinical and molecular genetic findings]. Nervenarzt (2011) 0.94
Development and validation of a bioreactor for physical stimulation of engineered cartilage. Biorheology (2003) 0.94
[Attitudes towards patient care at the end of life. A survey of directors of neurological departments]. Nervenarzt (2004) 0.94
The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case. Clin Genet (2010) 0.93
Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutation. Neuromuscul Disord (2005) 0.93
Orthogeriatric care pathway: a prospective survey of impact on length of stay, mortality and institutionalisation. Arch Orthop Trauma Surg (2014) 0.93
Predictive value of S-100beta and neuron-specific enolase serum levels for adverse neurologic outcome after cardiac surgery. J Thorac Cardiovasc Surg (2000) 0.93
Dynamic compression of cartilage constructs engineered from expanded human articular chondrocytes. Biochem Biophys Res Commun (2003) 0.92
New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle. J Neuropathol Exp Neurol (2000) 0.91
Frequency of calpain-3 c.550delA mutation in limb girdle muscular dystrophy type 2 and isolated hyperCKemia in German patients. Clin Neuropathol (2007) 0.91
Influence of oxygen ventilation on Doppler microemboli signals in patients with artificial heart valves. Stroke (1997) 0.91
Lack of dystrophin is associated with altered integration of the mitochondria and ATPases in slow-twitch muscle cells of MDX mice. Biochim Biophys Acta (2001) 0.90
Studies on the immune status of children with acute lymphocytic leukaemia. II. In remission with and without cytostatic treatment. Clin Exp Immunol (1976) 0.90
Molecular diagnosis of German patients with late-onset glycogen storage disease type II. J Inherit Metab Dis (2008) 0.89
Pure myopathy associated with a novel mitochondrial tRNA gene mutation. Neurology (2006) 0.89
Mitochondrial 3243 A-->G mutation (MELAS mutation) associated with painful muscle stiffness. Neuromuscul Disord (1999) 0.87
Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations. J Neurol (2011) 0.87
Molecular and biochemical investigations in fumarase deficiency. Mol Genet Metab (2006) 0.86
Treatment of tension-type headache with botulinum toxin: a pilot study. Eur J Med Res (1999) 0.86
Left ventricular wall thickness measurements by magnetic resonance: a validation study. Int J Card Imaging (1991) 0.86
Intra-individual comparison of human ankle and knee chondrocytes in vitro: relevance for talar cartilage repair. Osteoarthritis Cartilage (2008) 0.85
Compound heterozygosity for metachromatic leukodystrophy and arylsulfatase A pseudodeficiency alleles is not associated with progressive neurological disease. Am J Hum Genet (1993) 0.85
Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutation. Arch Neurol (2001) 0.85
Vitamin B12 transport in blood. I. Congenital deficiency of transcobalamin II. Blood (1975) 0.85
A gel model for measuring crystallization inhibitor activities. Urol Int (1983) 0.84
Age and sex dependency of carnitine concentration in human serum and skeletal muscle. Clin Chem (2001) 0.84
A specific point mutation in the mitochondrial genome of Caucasians with MELAS. Hum Genet (1991) 0.84
Laryngeal pleomorphic rhabdomyosarcoma. Auris Nasus Larynx (2007) 0.84
Distribution of pyruvate kinase type L and M2 in microdissected periportal and perivenous rat liver tissue with different dietary states. Hoppe Seylers Z Physiol Chem (1983) 0.84
No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation. J Neurol Neurosurg Psychiatry (2004) 0.84
A novel combination of mitochondrial tRNA and ND1 gene mutations in a syndrome with MELAS, cardiomyopathy, and diabetes mellitus. Hum Mutat (1996) 0.84
[Chronic progressive external ophthalmoplegia--symptom or syndrome?]. Klin Monbl Augenheilkd (2009) 0.84
[Sinonasal tract malignancies : a 14-year single institution experience]. HNO (2012) 0.83
Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes. J Neurol (1990) 0.83
Transcranial magnetic stimulation compared with upper motor neuron signs in patients with amyotrophic lateral sclerosis. J Neurol Sci (1999) 0.83
[Ocular involvement in MuSK antibody-positive myasthenia gravis]. Klin Monbl Augenheilkd (2006) 0.83
[Rhabdomyolysis and myoglobinuria]. Nervenarzt (2003) 0.83
Immersion and perfusion staining with 2,3,5-triphenyltetrazolium chloride (TTC) compared to mitochondrial enzymes 6 hours after MCA-occlusion in primates. Neurol Res (1994) 0.83
Reduced epicardial coronary vasodilator capacity in patients with left ventricular hypertrophy. Circulation (1995) 0.82
The role of histology and other risk factors for post-tonsillectomy haemorrhage. Eur Arch Otorhinolaryngol (2009) 0.82
Conformational state of a 25-mer peptide from the cyclophilin-binding loop of the HIV type 1 capsid protein. Biochem J (1997) 0.82
Mosaicism of dynein in spermatozoa and cilia and fibrous sheath aberrations in an infertile man. Andrologia (1983) 0.82
Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNA(Leu(UUR))]. FEBS Lett (1991) 0.82
[Open stabilization and primary hip arthroplasty in geriatric patients with acetabular fractures: combination of minimally invasive techniques]. Unfallchirurg (2011) 0.82
Inclusion body myositis: clinical and histopathological features of 36 patients. Clin Investig (1993) 0.82
SnapShot: Bioreactors systems in tissue engineering (TE) & regenerative medicine (RM). Biomaterials (2010) 0.82
Activation of epileptic foci by transcranial magnetic stimulation: effects on secretion of prolactin and luteinizing hormone. J Neurol (1990) 0.82
[Bilateral inferior hemianopsia as an early symptom of Heidenhain type Creutzfeldt-Jakob disease]. Klin Monbl Augenheilkd (2000) 0.81
Mutations in the gene for X-linked adrenoleukodystrophy in patients with different clinical phenotypes. Am J Hum Genet (1995) 0.81
Metabolic zonation in liver of diabetic rats. Zonal distribution of phosphoenolpyruvate carboxykinase, pyruvate kinase, glucose-6-phosphatase and succinate dehydrogenase. Biol Chem Hoppe Seyler (1985) 0.81
[Early treatment of acute myocardial infarct: implementation of therapy guidelines in routine clinical practice, MITRA pilot phase]. Z Kardiol (1997) 0.81
Probing substrate backbone function in prolyl oligopeptidase catalysis--large positional effects of peptide bond monothioxylation. Eur J Biochem (1997) 0.81
Unusual manifestations in two cases of necrotizing myopathy associated with SRP-antibodies. Clin Neurol Neurosurg (2012) 0.81
A novel implantation technique for engineered osteo-chondral grafts. Knee Surg Sports Traumatol Arthrosc (2009) 0.81
[Classical crossed pontine syndromes]. Fortschr Neurol Psychiatr (2004) 0.81
[Postpartum obturator nerve syndrome: case report and review of the nerve compression syndrome during pregnancy and delivery]. Zentralbl Gynakol (1997) 0.80
A novel nonsense mutation (R269X) in the myophosphorylase gene in a patient with McArdle disease. Mol Genet Metab (2001) 0.80
Mitochondrial encephalomyopathy: correlation of P-31 exercise MR spectroscopy with clinical findings. Radiology (1994) 0.80
[Age dependence of Doppler parameters in the basal cerebral arteries evaluated by transcranial color-coded duplex sonography. Reference data from 290 volunteers]. Fortschr Neurol Psychiatr (2003) 0.80
Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene. FEBS Lett (1993) 0.80
Heparin-binding epidermal growth factor-like growth factor: a component in chromaffin granules which promotes the survival of nigrostriatal dopaminergic neurones in vitro and in vivo. Neuroscience (2004) 0.80
Extended binding sites of cyclophilin as revealed by the interaction with HIV-1 Gag polyprotein derived oligopeptides. FEBS Lett (1996) 0.80
[Use of coronary angiography after acute myocardial infarction in Germany: a comparison of daily clinical practice with international guidelines. MITRA Study]. Z Kardiol (1999) 0.79
Cerebral MR in ophthalmoplegia plus. AJNR Am J Neuroradiol (1994) 0.79
Efalizumab-induced isolated cerebral lupus-like syndrome. Neurology (2009) 0.79
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndrome. Neurology (2005) 0.79