Published in Muscle Nerve on August 01, 1998
Abnormal muscle responses in hemifacial spasm: F waves or trigeminal reflexes? J Neurol Neurosurg Psychiatry (2006) 0.82
ERBIN: a basolateral PDZ protein that interacts with the mammalian ERBB2/HER2 receptor. Nat Cell Biol (2000) 2.90
Structural basis for discrimination of 3-phosphoinositides by pleckstrin homology domains. Mol Cell (2000) 2.86
[Peripheral neuropathies caused by perhexiline maleate. Apropos of 7 cases]. Coeur Med Interne (1977) 2.30
Risk factors and clinical relevance of nosocomial maxillary sinusitis in the critically ill. Am J Respir Crit Care Med (1994) 2.19
Evidence for interneuronally mediated Ia excitatory effects to human quadriceps motoneurones. J Physiol (1986) 2.15
Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities. Hum Mol Genet (2001) 2.08
Estimates of selection and gene flow from measures of cline width and linkage disequilibrium in heliconius hybrid zones. Genetics (1990) 2.05
X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study. Neurology (1998) 1.96
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A. Brain (2001) 1.82
Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23. Nat Genet (1996) 1.76
Pain in sciatica depresses lower limb nociceptive reflexes to sural nerve stimulation. J Neurol Neurosurg Psychiatry (1987) 1.71
Assessing the performance of single-copy genes for recovering robust phylogenies. Syst Biol (2008) 1.66
Use of linkage disequilibrium approaches to map genes for bipolar disorder in the Costa Rican population. Am J Med Genet (1996) 1.65
Psychophysical and electrophysiological approaches to the pain-relieving effects of heterotopic nociceptive stimuli. Brain (1984) 1.63
Genome-wide association study of obsessive-compulsive disorder. Mol Psychiatry (2012) 1.57
Assessing the feasibility of linkage disequilibrium methods for mapping complex traits: an initial screen for bipolar disorder loci on chromosome 18. Am J Hum Genet (1999) 1.54
Midbrain deafness with normal brainstem auditory evoked potentials. Neurology (2002) 1.51
Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness. Muscle Nerve (2000) 1.49
A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees. Proc Natl Acad Sci U S A (1996) 1.46
Genome-wide association study of Tourette's syndrome. Mol Psychiatry (2012) 1.42
Hereditary thermosensitive neuropathy: an autosomal dominant disorder of the peripheral nervous system. Neurology (1997) 1.42
Origin of malignant centrofacial granulomas: surface markers and gene rearrangement of malignant cells. Laryngoscope (1991) 1.40
Monthly intravenous pulse cyclophosphamide therapy in Wegener's granulomatosis. Clin Exp Rheumatol (1996) 1.39
Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination. Hum Mol Genet (1998) 1.38
Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion. Neurology (1999) 1.38
Comparative study of perceived pain and nociceptive flexion reflex in man. Pain (1977) 1.37
Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33. Hum Mol Genet (1996) 1.29
Cervical magnetic stimulation: a new painless method for bilateral phrenic nerve stimulation in conscious humans. J Appl Physiol (1985) (1989) 1.27
A re-evaluation of the pattern of group I fibre projections in the human lower limb on using randomly alternated stimulations. Exp Brain Res (1984) 1.27
Studies on pain. Effects of morphine on a spinal nociceptive flexion reflex and related pain sensation in man. Brain Res (1985) 1.26
Early neutrophil alveolitis after antigen inhalation in hypersensitivity pneumonitis. Chest (1985) 1.25
Diffuse noxious inhibitory controls (DNIC) in animals and in man. Patol Fiziol Eksp Ter (1993) 1.25
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis. Neurology (2004) 1.25
MR Imaging of the cervical cord in juvenile amyotrophy of distal upper extremity. AJNR Am J Neuroradiol (1989) 1.24
Descending control of reflex pathways in the production of voluntary isolated movements in man. Brain Res (1983) 1.20
Results and long-term followup of intravenous immunoglobulin infusions in chronic, refractory polymyositis: an open study with thirty-five adult patients. Arthritis Rheum (2002) 1.18
Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion. Neurology (1995) 1.18
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2. Neurology (2003) 1.18
Stress-induced analgesia in humans: endogenous opioids and naloxone-reversible depression of pain reflexes. Science (1981) 1.15
Sex-dependent rearrangements resulting in CMT1A and HNPP. Nat Genet (1997) 1.15
Parkinson's disease with camptocormia. J Neurol Neurosurg Psychiatry (2006) 1.14
Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies. Neuromuscul Disord (2000) 1.13
Follow-up study and response to treatment in 23 patients with Lewis-Sumner syndrome. Brain (2004) 1.12
Abnormal pattern of cerebral blood flow distribution in young alcohol addicts. Br J Addict (1988) 1.12
Validity of diagnostic criteria for chronic inflammatory demyelinating polyneuropathy: a multicentre European study. J Neurol Neurosurg Psychiatry (2009) 1.10
[Acute digitalis poisoning (70 cases)]. Bull Mem Soc Med Hop Paris (1969) 1.10
Intravenous immunoglobulin therapy in multifocal motor neuropathy: a double-blind, placebo-controlled study. Brain (2001) 1.09
Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutation. Neurology (2010) 1.05
European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of multifocal motor neuropathy. Eur J Neurol (2006) 1.04
Supraspinal influences on nociceptive flexion reflex and pain sensation in man. Brain Res (1979) 1.04
Hepatitis C virus infection with peripheral neuropathy is not always associated with cryoglobulinaemia. Ann Rheum Dis (2001) 1.04
Cutaneous facilitation of transmission in Ib reflex pathways in the human upper limb. Exp Brain Res (1985) 1.04
Diffuse noxious inhibitory controls in man. Involvement of the spinoreticular tract. Brain (1990) 1.03
Severe perturbations of the blood T cell repertoire in polymyositis, but not dermatomyositis patients. J Immunol (2001) 1.03
[Letter: 7 peripheral neuropathies after treatment by perhexiline maleate]. Nouv Presse Med (1976) 1.03
Peripheral neuropathy associated with IgM monoclonal gammopathy: correlations between M-protein antibody activity and clinical/electrophysiological features in 40 cases. Muscle Nerve (1998) 1.03
Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene. Neuromuscul Disord (2008) 1.02
Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature. Brain (2001) 1.02
Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease. Brain (2001) 1.02
Neuropathy in lymphoma: a relationship between the pattern of neuropathy, type of lymphoma and prognosis? J Neurol Neurosurg Psychiatry (2007) 1.01
Estimation of national colorectal-cancer incidence using claims databases. J Cancer Epidemiol (2012) 1.00
The late open artery hypothesis--a decade later. Am Heart J (2001) 0.99
Superoxide anion generation by alveolar inflammatory cells in simple pneumoconiosis and in progressive massive fibrosis of nonsmoking coal workers. Am Rev Respir Dis (1990) 0.99
Systemic vasculitis in patients with hepatitis C. J Rheumatol (2001) 0.99
In vitro characterization of naturally occurring influenza H3NA- viruses lacking the NA gene segment: toward a new mechanism of viral resistance? Virology (2010) 0.99
Nociceptive flexion reflexes elicited by noxious laser radiant heat in man. Pain (1979) 0.99
Population genetics of fungal diseases of plants. Parasite (2008) 0.99
An electrophysiological investigation into the monosynaptic H-reflex in the rat. Brain Res (1998) 0.99
The phenomenology of body image distortions induced by regional anaesthesia. Brain (2003) 0.99
[Study of antiglycolipid antibodies in IgM monoclonal dysglobulinemias associated with peripheral neuropathy]. Rev Neurol (Paris) (1988) 0.98
The spectrum of polyneuropathies in patients infected with HIV. J Neurol Neurosurg Psychiatry (1989) 0.98
Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene. Am J Hum Genet (2000) 0.98
Painful and painless peripheral sensory neuropathies due to HIV infection: a comparison using quantitative sensory evaluation. Pain (1999) 0.98
[Poisoning by tricyclic antidepressive agents]. Therapie (1974) 0.97
Verification of biomechanical methods employed in a comprehensive study of mild traumatic brain injury and the effectiveness of American football helmets. J Biomech (2005) 0.97
A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2? Hum Mol Genet (1996) 0.97
Miller Fisher syndrome: clinical and electrophysiologic evidence of peripheral origin in 10 cases. Neurology (1984) 0.96
Chronic dysimmune demyelinating polyneuropathy: a clinical and electrophysiological study of 93 patients. J Neurol Neurosurg Psychiatry (1996) 0.96
Congenital insensitivity to pain, and endogenous morphine-like substances. Lancet (1977) 0.96
Aspirin-sensitive asthma: abnormal platelet response to drugs inducing asthmatic attacks. Diagnostic and physiopathological implications. Int Arch Allergy Appl Immunol (1985) 0.96
Vivid dreams, hallucinations, psychosis and REM sleep in Guillain-Barré syndrome. Brain (2005) 0.96
Electrophysiological evidence for a facio-facial reflex in the facial muscles in man. Brain Res (1977) 0.95
Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11. J Med Genet (2005) 0.95
Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group. J Med Genet (1992) 0.95
Diagnostic value of markers of muscle degeneration in sporadic inclusion body myositis. Acta Myol (2011) 0.95