Published in Clin Sci (Lond) on July 01, 2001
StO₂ guided early resuscitation in subjects with severe sepsis or septic shock: a pilot randomised trial. J Clin Monit Comput (2013) 1.51
Cutaneous Respirometry as Novel Technique to Monitor Mitochondrial Function: A Feasibility Study in Healthy Volunteers. PLoS One (2016) 1.39
Near-infrared spectroscopy technique to evaluate the effects of red blood cell transfusion on tissue oxygenation. Crit Care (2009) 1.14
Dual gradient-echo MRI of post-contraction changes in skeletal muscle blood volume and oxygenation. Magn Reson Med (2007) 1.10
Effects of muscle fiber motion on diffuse correlation spectroscopy blood flow measurements during exercise. Biomed Opt Express (2010) 1.07
Absolute and relative contributions of BOLD effects to the muscle functional MRI signal intensity time course: effect of exercise intensity. Magn Reson Med (2007) 1.06
Skeletal muscle StO2 kinetics are slowed during low work rate calf exercise in peripheral arterial disease. Eur J Appl Physiol (2007) 1.04
Noninvasive evaluation of skeletal muscle mitochondrial capacity with near-infrared spectroscopy: correcting for blood volume changes. J Appl Physiol (1985) (2012) 1.04
Pattern of deoxy[Hb+Mb] during ramp cycle exercise: influence of aerobic fitness status. Eur J Appl Physiol (2009) 1.02
Intraoperative evaluation of revascularization effect on ischemic muscle hemodynamics using near-infrared diffuse optical spectroscopies. J Biomed Opt (2011) 1.00
Near-infrared assessments of skeletal muscle oxidative capacity in persons with spinal cord injury. Eur J Appl Physiol (2013) 0.94
Skin blood flow differentially affects near-infrared spectroscopy-derived measures of muscle oxygen saturation and blood volume at rest and during dynamic leg exercise. Eur J Appl Physiol (2010) 0.94
Assessment of in vivo skeletal muscle mitochondrial respiratory capacity in humans by near-infrared spectroscopy: a comparison with in situ measurements. J Physiol (2014) 0.90
Modeling oxygenation in venous blood and skeletal muscle in response to exercise using near-infrared spectroscopy. J Appl Physiol (1985) (2009) 0.90
Near infrared spectroscopy (NIRS) of the thenar eminence in anesthesia and intensive care. Ann Intensive Care (2012) 0.87
Relationship between erector spinae static endurance and muscle oxygenation-blood volume changes in healthy and low back pain subjects. Eur J Appl Physiol (2005) 0.85
Microcirculatory changes and skeletal muscle oxygenation measured at rest by non-infrared spectroscopy in patients with and without diabetes undergoing haemodialysis. Crit Care (2009) 0.84
Changes in skeletal muscle oxygenation during exercise measured by near-infrared spectroscopy on ascent to altitude. Crit Care (2009) 0.84
Is leg compression beneficial for alpine skiers? BMC Sports Sci Med Rehabil (2013) 0.84
Muscle oxygen changes following Sprint Interval Cycling training in elite field hockey players. PLoS One (2015) 0.83
Age and microvascular responses to knee extensor exercise in women. Eur J Appl Physiol (2008) 0.83
Normal muscle oxygen consumption and fatigability in sickle cell patients despite reduced microvascular oxygenation and hemorheological abnormalities. PLoS One (2012) 0.82
Association between regional quadriceps oxygenation and blood oxygen saturation during normoxic one-legged dynamic knee extension. Eur J Appl Physiol (2005) 0.82
Detection of changes in muscle oxygen saturation in the human leg: a comparison of two near-infrared spectroscopy devices. J Clin Monit Comput (2013) 0.82
500 ml of blood loss does not decrease non-invasive tissue oxygen saturation (StO2) as measured by near infrared spectroscopy - A hypothesis generating pilot study in healthy adult women. J Trauma Manag Outcomes (2010) 0.80
Knee angle-dependent oxygen consumption of human quadriceps muscles during maximal voluntary and electrically evoked contractions. Eur J Appl Physiol (2007) 0.80
Wavelet analysis of lumbar muscle oxygenation signals during whole-body vibration: implications for the development of localized muscle fatigue. Eur J Appl Physiol (2012) 0.80
Investigation of spectral interferences on the accuracy of broadband CW-NIRS tissue SO(2) determination. Biomed Opt Express (2010) 0.79
Electromyographic, cerebral, and muscle hemodynamic responses during intermittent, isometric contractions of the biceps brachii at three submaximal intensities. Front Physiol (2014) 0.79
Cardiac troponin and skeletal muscle oxygenation in severe post-partum haemorrhage. Crit Care (2009) 0.79
Influence of posture on pulmonary o2 uptake kinetics, muscle deoxygenation and myolectrical activity during heavy-intensity exercise. J Sports Sci Med (2006) 0.79
Pulmonary oxygen uptake and muscle deoxygenation kinetics during recovery in trained and untrained male adolescents. Eur J Appl Physiol (2011) 0.78
The relationship between oxygenation and myoelectric activity in the forearm and shoulder muscles of males and females. Eur J Appl Physiol (2010) 0.78
Cardiorespiratory and hemodynamic responses during repetitive incremental lifting and lowering in healthy males and females. Eur J Appl Physiol (2003) 0.77
Effects of time pressure and precision demands during computer mouse work on muscle oxygenation and position sense. Eur J Appl Physiol (2005) 0.77
Oxygenation, local muscle oxygen consumption and joint specific power in cycling: the effect of cadence at a constant external work rate. Eur J Appl Physiol (2016) 0.77
Effect of opioid administration on cardiorespiratory and muscle oxygenation during lifting in chronic back pain patients. Eur J Appl Physiol (2010) 0.77
Tolerance to high-intensity intermittent running exercise: do oxygen uptake kinetics really matter? Front Physiol (2012) 0.77
Knee extensor muscle oxygen consumption in relation to muscle activation. Eur J Appl Physiol (2006) 0.77
Factors associated with a low initial cerebral oxygen saturation value in patients undergoing cardiac surgery. J Artif Organs (2017) 0.77
Effects of therapeutic ultrasound on intramuscular blood circulation and oxygen dynamics. J Jpn Phys Ther Assoc (2014) 0.76
Exploring the vascular smooth muscle receptor landscape in vivo: ultrasound Doppler versus near-infrared spectroscopy assessments. Am J Physiol Heart Circ Physiol (2014) 0.76
Comparison of oxygenation in peripheral muscle during submaximal aerobic exercise, in persons with COPD and healthy, matched-control persons. Int J Chron Obstruct Pulmon Dis (2006) 0.76
Calibration of diffuse correlation spectroscopy blood flow index with venous-occlusion diffuse optical spectroscopy in skeletal muscle. J Biomed Opt (2015) 0.76
Oxygenation and hemodynamics do not underlie early muscle fatigue for patients with work-related muscle pain. PLoS One (2014) 0.76
Effects of Cold Water Immersion on Muscle Oxygenation During Repeated Bouts of Fatiguing Exercise: A Randomized Controlled Study. Medicine (Baltimore) (2016) 0.75
Recent developments in near-infrared spectroscopy (NIRS) for the assessment of local skeletal muscle microvascular function and capacity to utilise oxygen. Artery Res (2016) 0.75
The Effect of Short and Long Term Endurance Training on Systemic, and Muscle and Prefrontal Cortex Tissue Oxygen Utilisation in 40 - 60 Year Old Women. PLoS One (2016) 0.75
Oxygenation Threshold Derived from Near-Infrared Spectroscopy: Reliability and Its Relationship with the First Ventilatory Threshold. PLoS One (2016) 0.75
Relationship of post-exercise muscle oxygenation and duration of cycling exercise. BMC Sports Sci Med Rehabil (2016) 0.75
An integrated view on the oxygenation responses to incremental exercise at the brain, the locomotor and respiratory muscles. Eur J Appl Physiol (2016) 0.75
In Vivo Assessment of Mitochondrial Dysfunction in Clinical Populations Using Near-Infrared Spectroscopy. Front Physiol (2017) 0.75
Forearm muscle oxidative capacity index predicts sport rock-climbing performance. Eur J Appl Physiol (2016) 0.75
Influence of exercise duration on cardiorespiratory responses, energy cost and tissue oxygenation within a 6 hour treadmill run. PeerJ (2017) 0.75
The frequency of lysosomal storage diseases in The Netherlands. Hum Genet (1999) 3.54
Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene. Am J Hum Genet (1998) 2.62
Role of cobalamin intake and atrophic gastritis in mild cobalamin deficiency in older Dutch subjects. Am J Clin Nutr (1998) 2.26
Dimethylmethylene blue-based spectrophotometry of glycosaminoglycans in untreated urine: a rapid screening procedure for mucopolysaccharidoses. Clin Chem (1989) 1.91
Performance of near-infrared spectroscopy in measuring local O(2) consumption and blood flow in skeletal muscle. J Appl Physiol (1985) (2001) 1.86
Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy. Neurology (2010) 1.80
Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation. Eur J Hum Genet (2007) 1.76
Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis. Brain (2000) 1.75
A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome. Ann Neurol (1993) 1.70
Cerebrotendinous xanthomatosis: the spectrum of imaging findings and the correlation with neuropathologic findings. Radiology (2000) 1.63
Mitochondrial creatine kinase: a key enzyme of aerobic energy metabolism. Biochim Biophys Acta (1992) 1.59
Genetic characteristics of myoadenylate deaminase deficiency. Ann Neurol (1998) 1.57
Idiopathic neuralgic amyotrophy in children. A distinct phenotype compared to the adult form. Neuropediatrics (2000) 1.50
Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency? Neurology (2008) 1.45
Tyrosine hydroxylase deficiency with severe clinical course: clinical and biochemical investigations and optimization of therapy. J Pediatr (2000) 1.45
Improved vision after intravenous immunoglobulin in stable demyelinating optic neuritis. Ann Neurol (1992) 1.44
Proton nuclear magnetic resonance spectroscopy of body fluids in the field of inborn errors of metabolism. Ann Clin Biochem (2003) 1.42
[The anti-synthetase syndrome: muscle disease and multisystem disorder at the same time]. Ned Tijdschr Geneeskd (2003) 1.38
[Clinical reasoning and decision making in practice. A 23 year old woman with malaise, anorexia, fever and behavior changes]. Ned Tijdschr Geneeskd (2004) 1.38
Juvenile cataract associated with chronic diarrhea in pediatric cerebrotendinous xanthomatosis. Am J Ophthalmol (1991) 1.38
Measuring urinary glycosaminoglycans in the presence of protein: an improved screening procedure for mucopolysaccharidoses based on dimethylmethylene blue. Clin Chem (1992) 1.34
A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic. Proc Natl Acad Sci U S A (1999) 1.33
Elevated plasma chitotriosidase activity in various lysosomal storage disorders. J Inherit Metab Dis (1995) 1.28
Dopa-responsive dystonia: a clinical and molecular genetic study. Ann Neurol (1998) 1.25
Meningoencephalitis caused by Streptococcus pneumoniae: a diagnostic and therapeutic challenge. Diagnosis with diffusion-weighted MRI leading to treatment with corticosteroids. Neuroradiology (2005) 1.25
Congenital disorder of glycosylation type Ix: review of clinical spectrum and diagnostic steps. J Inherit Metab Dis (2008) 1.23
Cerebellar ataxia and congenital disorder of glycosylation Ia (CDG-Ia) with normal routine CDG screening. J Neurol (2007) 1.23
Ophthalmological abnormalities in children with congenital disorders of glycosylation type I. Br J Ophthalmol (2008) 1.21
Sporadic late-onset nemaline myopathy effectively treated by melphalan and stem cell transplant. Neurology (2008) 1.20
Ocular and systemic manifestations of cerebrotendinous xanthomatosis. Am J Ophthalmol (1995) 1.18
Clinical and genetic spectrum of Sanfilippo type C (MPS IIIC) disease in The Netherlands. Mol Genet Metab (2007) 1.18
Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosis. Brain (1999) 1.17
Orthostatic tolerance, cerebral oxygenation, and blood velocity in humans with sympathetic failure. Stroke (2000) 1.17
Severe hypomyelination associated with increased levels of N-acetylaspartylglutamate in CSF. Neurology (2004) 1.10
Intestinal permeability after severe trauma and hemorrhagic shock is increased without relation to septic complications. Arch Surg (1993) 1.10
Treatment and follow-up of children with cerebrotendinous xanthomatosis. Eur J Pediatr (1998) 1.10
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesis. Ann Neurol (2000) 1.09
Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency. Am J Hum Genet (2001) 1.09
Biochemical hallmarks of tyrosine hydroxylase deficiency. Clin Chem (1998) 1.09
Simvastatin. A new therapeutic approach for Smith-Lemli-Opitz syndrome. J Lipid Res (2000) 1.09
Mevalonate kinase deficiency: Evidence for a phenotypic continuum. Neurology (2004) 1.08
Becoming a research-oriented family physician. Fam Med (2005) 1.06
Leukoencephalopathy associated with a disturbance in the metabolism of polyols. Ann Neurol (1999) 1.06
Clinical and serological characteristics of 125 Dutch myositis patients. Myositis specific autoantibodies aid in the differential diagnosis of the idiopathic inflammatory myopathies. J Neurol (2002) 1.05
Multi-allelic origin of congenital disorder of glycosylation (CDG)-Ic. Hum Genet (2000) 1.05
Age-related changes of neuron-specific enolase, S-100 protein, and myelin basic protein concentrations in cerebrospinal fluid. Clin Chem (1992) 1.05
Acceleration in the rate of CNS remyelination in lysolecithin-induced demyelination. J Neurosci (1998) 1.03
Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin pattern. Biochim Biophys Acta (2011) 1.03
Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter. J Child Neurol (1999) 1.03
DBH gene variants that cause low plasma dopamine beta hydroxylase with or without a severe orthostatic syndrome. J Med Genet (2004) 1.02
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic value. Hum Mutat (1997) 1.02
Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype. J Med Genet (1996) 1.01
Myositis-specific autoantibodies: overview and recent developments. Curr Opin Rheumatol (2001) 1.01
Near infrared spectroscopy for noninvasive assessment of claudication. J Surg Res (1997) 1.00
Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A gene. J Med Genet (1996) 1.00
Cerebral oxygenation declines in healthy elderly subjects in response to assuming the upright position. Stroke (2000) 0.99
Technical and biochemical factors affecting cerebrospinal fluid 5-MTHF, biopterin and neopterin concentrations. Mol Genet Metab (2008) 0.99
Clinical and molecular overlap between myopathies and inherited connective tissue diseases. Neuromuscul Disord (2008) 0.99
Defect in dimethylglycine dehydrogenase, a new inborn error of metabolism: NMR spectroscopy study. Clin Chem (1999) 0.99
The relative prevalence of dermatomyositis and polymyositis in Europe exhibits a latitudinal gradient. Ann Rheum Dis (2000) 0.98
Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease. Neurology (1996) 0.98
A branch site mutation leading to aberrant splicing of the human tyrosine hydroxylase gene in a child with a severe extrapyramidal movement disorder. Ann Hum Genet (2000) 0.97
Clinical and biochemical presentation of siblings with COG-7 deficiency, a lethal multiple O- and N-glycosylation disorder. J Inherit Metab Dis (2005) 0.97
Intestinal permeability is increased after major vascular surgery. J Vasc Surg (1993) 0.96
Congenital nephrotic syndrome: a novel phenotype of type I carbohydrate-deficient glycoprotein syndrome. J Inherit Metab Dis (1996) 0.96
Clinical imaging and neuropathological correlations in an unusual case of cerebrotendinous xanthomatosis. Clin Neuropathol (2010) 0.96
The natural history of hereditary neuralgic amyotrophy in the Dutch population: two distinct types? Brain (2000) 0.95
Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patients. Neuromuscul Disord (2000) 0.95
Aromatic L-amino acid decarboxylase deficiency with hyperdopaminuria. Clinical and laboratory findings in response to different therapies. Neuropediatrics (2002) 0.95
Aromatic L-amino acid decarboxylase enzyme activity in deficient patients and heterozygotes. Mol Genet Metab (2007) 0.95
Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation. Brain (1998) 0.95
Two new mutations in the sterol 27-hydroxylase gene in two families lead to cerebrotendinous xanthomatosis. Hum Genet (1996) 0.95
Skeletal dysplasia with brachytelephalangy in a patient with a congenital disorder of glycosylation due to ALG6 gene mutations. Clin Genet (2010) 0.94
Clinical symptoms of adult metachromatic leukodystrophy and arylsulfatase A pseudodeficiency. Arch Neurol (1995) 0.94
Six novel mutations in the alpha-galactosidase A gene in families with Fabry disease. Hum Mol Genet (1994) 0.94
Infantile Parkinsonism-dystonia and elevated dopamine metabolites in CSF. Neurology (2004) 0.94
Cerebrospinal neuron-specific enolase, S-100 and myelin basic protein in neurological disorders. Acta Neurol Scand (1995) 0.94
Pitfalls in measuring plasma cholesterol in the Smith-Lemli-Opitz syndrome. Clin Chem (1997) 0.93
Ca2+ homeostasis in Brody's disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamil. J Clin Invest (1994) 0.93
Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith--Lemli--Opitz syndrome. Ann Hum Genet (2001) 0.93
Effect of simvastatin in addition to chenodeoxycholic acid in patients with cerebrotendinous xanthomatosis. Metabolism (1999) 0.93
Ehlers-Danlos syndrome due to tenascin-X deficiency: muscle weakness and contractures support overlap with collagen VI myopathies. Am J Med Genet A (2007) 0.92
Cerebrospinal fluid investigations for neurometabolic disorders. Neuropediatrics (1998) 0.92
Isolated eyelid closure myotonia in two families with sodium channel myotonia. Neurogenetics (2009) 0.92
Smith-Lemli-Opitz syndrome and the DHCR7 gene. Ann Hum Genet (2003) 0.92
The spot test is not a reliable screening procedure for mucopolysaccharidoses. Clin Chem (1991) 0.92
New cases of adult-onset Sandhoff disease with a cerebellar or lower motor neuron phenotype. J Neurol Neurosurg Psychiatry (2010) 0.91
Improvement of screening in exertional myalgia with a standardized ischemic forearm test. Muscle Nerve (1986) 0.91
Substrate deprivation therapy in juvenile Sandhoff disease. J Inherit Metab Dis (2009) 0.91
Clinical findings and a therapeutic trial in the first patient with beta-ureidopropionase deficiency. Neuropediatrics (2006) 0.91
Phenotypic expression in mucopolysaccharidosis VII. J Neurol Neurosurg Psychiatry (1987) 0.91
Presence of diarrhea and absence of tendon xanthomas in patients with cerebrotendinous xanthomatosis. Arch Neurol (2000) 0.90