Published in J Pediatr on December 01, 1968
Premedication for jejunal biopsy in childhood using intravenous diazepam and metoclopramide. Arch Dis Child (1974) 0.88
Valium in the treatment of epilepsy. Calif Med (1970) 0.85
Uraemia as a determinant of convulsions in acute infantile hypernatraemia. Arch Dis Child (1971) 0.79
Diseases of the central nervous system: Epilepsy. Br Med J (1975) 0.75
Recombinant-inbred strains. An aid to finding identity, linkage, and function of histocompatibility and other genes. Transplantation (1971) 6.02
Letter: Ampicillin-resistant Haemophilus influenzae meningitis. Lancet (1974) 5.33
Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy. N Engl J Med (1989) 3.32
Risk of seizures and encephalopathy after immunization with the diphtheria-tetanus-pertussis vaccine. JAMA (1990) 2.54
Neurological complications of immunization. Ann Neurol (1982) 2.25
Clinical, bacteriological, and immunological characterisation of ampicillin-resistant Haemophilus influenzae type B. Lancet (1974) 2.14
Clinical trial in Duchenne dystrophy. I. The design of the protocol. Muscle Nerve (1981) 2.06
Genes for immunoglobulin heavy chain and serum prealbumin protein are linked in mouse. Nature (1975) 2.01
Clinical investigation in Duchenne dystrophy: 2. Determination of the "power" of therapeutic trials based on the natural history. Muscle Nerve (1983) 1.99
Duchenne muscular dystrophy: patterns of clinical progression and effects of supportive therapy. Neurology (1989) 1.90
Prednisone in Duchenne dystrophy. A randomized, controlled trial defining the time course and dose response. Clinical Investigation of Duchenne Dystrophy Group. Arch Neurol (1991) 1.78
Duchenne dystrophy: randomized, controlled trial of prednisone (18 months) and azathioprine (12 months) Neurology (1993) 1.75
The natural history of acute confusional migraine. Arch Neurol (1978) 1.66
Allelic forms of a gene controlling the female immune response to the male antigen in mice. Transplantation (1971) 1.65
Inherited histocompatibility changes in progeny of irradiated and unirradiated inbred mice. Genet Res (1965) 1.58
Risk of seizures after measles-mumps-rubella immunization. Pediatrics (1991) 1.43
Recombinant inbred lines: value in the genetic analysis of biochemical variants. Science (1973) 1.42
Neurogenic atrophy simulating facioscapulohumeral dystrophy. A dominant form. Arch Neurol (1967) 1.39
A gene governing the female immune response to the male antigen in mice. Transplantation (1971) 1.37
Normal median nerve proximal latency in carpal tunnel syndrome: a clue to coexisting Martin-Gruber anastomosis. J Neurol Neurosurg Psychiatry (1976) 1.34
Genomic analysis of the C57BL/Ks mouse strain. Mamm Genome (1995) 1.30
Ly-4, a new locus determining a lymphocyte cell-surface alloantigen in mice. Proc Natl Acad Sci U S A (1973) 1.30
The non-H-2 histocompatibility loci and their antigens. Transplant Rev (1973) 1.29
Genes that affect morphogenesis of the murine mandible. Recombinant-inbred strain analysis. J Hered (1986) 1.25
A model for genetic analysis of programmed gene expression as reflected in the development of membrane antigens. Dev Biol (1975) 1.25
Nonsense and missense mutations of the muscle chloride channel gene in patients with myotonia congenita. Hum Mol Genet (1994) 1.22
Intracranial hemorrhage in the term newborn. Arch Neurol (1984) 1.22
T-lymphocyte response to H-2 mutants. I. Proliferation is dependent on Ly 1+2+ cells. J Exp Med (1978) 1.21
Genes that affect the shape of the murine mandible. Congenic strain analysis. J Hered (1985) 1.20
Clinical investigation of Duchenne muscular dystrophy. Interesting results in a trial of prednisone. Arch Neurol (1987) 1.14
A spinal muscular atrophy with scapuloperoneal distribution. Arch Neurol (1968) 1.11
Muscle lesions in myasthenia gravis. Ann N Y Acad Sci (1966) 1.09
Using an EPID for patient-specific VMAT quality assurance. Med Phys (2011) 1.08
Clinical syndromes of myasthenia in infancy and childhood. A review. Arch Neurol (1978) 1.08
Histocompatibility differences in wild mice; further evidence for the existence of deme structure in natural populations of the house mouse. Genetics (1971) 1.08
T lymphocyte response to H-2 mutants: cytotoxic effectors are Ly-1+2+. Proc Natl Acad Sci U S A (1979) 1.07
Chronic inhibition of cholinesterase as a cause of myopathy. Neurology (1972) 1.07
Major urinary protein and immunoglobulin allotypes of recombinant inbred mouse strains. Genet Res (1973) 1.06
Estimates of the number of loci contributing to the histoincompatibility between C57BL-6 and BALB-c strains of mice. Transplantation (1969) 1.05
Pediatric manifestations of Hashimoto's encephalopathy. Pediatr Neurol (1999) 1.04
Clinical investigation of Duchenne muscular dystrophy. A methodology for therapeutic trials based on natural history controls. Arch Neurol (1987) 1.02
A crucial role of the H-2 D locus in the regulation of both the D- and the K-associated cytotoxic T lymphocyte response against Moloney leukemia virus, demonstrated with two Db mutants. J Immunol (1982) 1.01
Two syndromes following rubella immunization. Clinical observations and epidemiological studies. JAMA (1970) 1.01
The effects of weaning beef calves in two stages on their behavior and growth rate. J Anim Sci (2005) 1.00
Hypoxic-ischemic encephalopathy in the newborn. Arch Neurol (1983) 1.00
An autosomal-dominant dystrophy with humeropelvic distribution and cardiomyopathy. Neurology (1982) 0.99
The pregnant epileptic: a review and recommendations. Arch Neurol (1979) 0.99
Genetics of susceptibility to plasmacytoma induction. I. BALB/cAnN (C), C57BL/6N (B6), C57BL/Ka (BK), (C times B6)F1, (C times BK)F1, and C times B recombinant-inbred strains. J Natl Cancer Inst (1975) 0.99
Agenesis of the corpus callosum. Arch Neurol (1980) 0.98
Clinical investigation in Duchenne dystrophy: V. Use of creatine kinase and pyruvate kinase in carrier detection. Muscle Nerve (1985) 0.98
Incidence and prognosis of seizures in infants after cardiac surgery with profound hypothermia and circulatory arrest. JAMA (1984) 0.97
The male antigen. II. Regulation of the primary and secondary responses to H-Y by H-2 associated genes. Cell Immunol (1974) 0.97
A locus affecting circulating interferon levels induced by mouse mammary tumour virus. J Gen Virol (1974) 0.96
Surgical disconnection of the cerebral hemispheres for intractable seizures. Results in infancy and childhood. JAMA (1970) 0.96
Location of Ly-7 on mouse chromosome 12. Immunogenetics (1984) 0.96
Heritable histocompatibility changes: lysogeny in mice? Transplantation (1966) 0.95
Treatment of salmonella meningitis. Clin Proc Child Hosp Dist Columbia (1969) 0.95
Studies on neuromelanin. II. Melanin in the brainstems of infants and children. Neurology (1968) 0.95
Juvenile Parkinsonism treated with levodopa. Arch Neurol (1972) 0.94
Genetic correlation between open-field activity and defecation: analysis with the CXB recombinant-inbred strains. Behav Genet (1979) 0.94
Studies on neuromelanin. I. A melanin system in the human adult brainstem. Neurology (1967) 0.93
Location of histocompatibility and interferon loci on chromosome 3 of the mouse. J Hered (1984) 0.92
Difference between two inbred strains of mice in ovulatory response to repeated administration of gonadotrophins. J Reprod Fertil (1965) 0.92
Thymectomy for the myasthenia gravis patient: factors influencing outcome. Ann Thorac Surg (1994) 0.92
T-cell subsets in polymyositis. Ann Neurol (1983) 0.91
Genetic analyses of differences in incidence of mammary tumors and reticulum cell neoplasms with the use of recombinant inbred lines of mice. J Natl Cancer Inst (1978) 0.91
Epidural hematoma of the newborn due to birth trauma. Pediatr Neurol (1989) 0.91
Migraine as a cause of benign paroxysmal vertigo of childhood. J Pediatr (1967) 0.89
Studies of two H-2Db mutants: B6. C-H-2bm13 and B6.C-H-2bm14. Immunogenetics (1980) 0.88
Three new mutations in patients with myophosphorylase deficiency (McArdle disease). Am J Hum Genet (1994) 0.88
Contemporary management of myasthenia gravis: the clinical role of thymectomy. Ann Thorac Surg (1977) 0.88
Immunodominance in the immune response to "multiple" histocompatibility antigens. Immunogenetics (1982) 0.87
Genetic programming of development: a model. Differentiation (1986) 0.87
Opiate receptors in mice: genetic differences. Life Sci (1975) 0.87
The natural history of Duchenne muscular dystrophy: a caveat for therapeutic trials. Trans Am Neurol Assoc (1981) 0.86
Genes on different chromosomes influence the antibody response to bacterial antigens. Immunogenetics (1985) 0.85
Clinical investigation in Duchenne dystrophy. VI. Double-blind controlled trial of nifedipine. Muscle Nerve (1987) 0.85
Genetic heterogeneity in Duchenne dystrophy. Ann Neurol (1987) 0.84
Exploratory activity: genetic analysis of its modification by scopolamine and amphetamine. Physiol Behav (1973) 0.84
An experimental myopathy secondary to excessive acetylcholine release. Neurology (1974) 0.84
Genetics of histocompatibility in mice. III. Characteristics of the popliteal lymph-node response to minor (non-H-2) H antigens. Immunogenetics (1981) 0.83
Recent clinical advances in the treatment of neurological diseases. Pediatr Clin North Am (1970) 0.82
Abnormalities of skeletal muscle maturation in brain damaged children: a histochemical study. Dev Med Child Neurol (1967) 0.82
Genetics of histocompatibility in mice. II. Survey for interactions between minor (non-H-2) antigens by skin grafting. Immunogenetics (1980) 0.81
Cerebral influence on muscle fiber typing. The effect of fetal immobilization. Arch Neurol (1969) 0.81
Homocystinuria. Clin Proc Child Hosp Dist Columbia (1969) 0.81
The pertussis vaccine controversy. The danger of case reports. Arch Neurol (1983) 0.81
Heart rate changes in convulsive and nonconvulsive neonatal apnea. Ann Neurol (1980) 0.80
Genetic drift: the problem and its possible solution by frozen-embryo storage. Ciba Found Symp (1978) 0.80
Pimozide treatment of Sydenham's chorea. Neurology (1990) 0.79
Histocompatibility of skin grafts from mice of F1, F2, and F3 generations on F1 generation hosts. Transplantation (1969) 0.79
Rapid mutations in mice? Science (1985) 0.79
Cramps, muscle pain, and tubular aggregates. Arch Neurol (1980) 0.79
Genetic analysis of plasma corticosterone levels in two inbred strains of mice. J Endocrinol (1972) 0.79
Brachial neuritis following routine childhood immunization for diphtheria, tetanus, and pertussis (DTP): report of two cases and review of the literature. Pediatrics (1997) 0.78
Interaction of H-2Db with mutant histocompatibility gene H (KH-11) in the mouse. Immunogenetics (1980) 0.78
Superoxide dismutases, glutathione peroxidase, and catalase in neuromuscular disease. Muscle Nerve (1987) 0.78
Clinical investigation in Duchenne muscular dystrophy: IV. Double-blind controlled trial of leucine. Muscle Nerve (1984) 0.78