Published in Arch Neurol on April 01, 1978
Neonatal form of dystrophia myotonica. Five cases in preterm babies and a review of earlier reports. Arch Dis Child (1979) 1.24
Don't it make my blue eyes brown: heterochromia and other abnormalities of the iris. Eye (Lond) (2011) 0.94
Transient monocular obscuration--?amaurosis fugax: a case report. Br J Ophthalmol (1985) 0.91
Restless legs syndrome. West J Med (1986) 2.39
Ocular manifestations in the Marfan syndrome and homocystinuria. Am J Ophthalmol (1973) 2.01
Type II syndactyly. Am J Hum Genet (1968) 1.85
The Rieger syndrome. Am J Med Genet (1978) 1.61
The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting. Arch Neurol (1967) 1.57
Electro-oculography in Best's macular dystrophy. Am J Ophthalmol (1974) 1.53
Congenital anomalies in Duane's retraction syndrome. Arch Ophthalmol (1972) 1.42
Adult-onset acid maltase deficiency: a postmortem study. Muscle Nerve (1979) 1.33
Ectopia lentis et pupillae. Am J Ophthalmol (1979) 1.24
Population studies and the Old Order Amish. Nature (1976) 1.21
Hyperthyroid myopathy. Intracellular electrophysiological measurements in biopsied human intercostal muscle. J Neurol Sci (1975) 1.20
The mast syndrome. A recessively inherited form of presenile dementia with motor disturbances. Arch Neurol (1967) 1.18
Ocular complications in the Weill-Marchesani syndrome. Am J Ophthalmol (1974) 1.17
A new oculocerebral syndrome with hypopigmentation. J Pediatr (1967) 1.13
Debrancher deficiency: neuromuscular disorder in 5 adults. Ann Neurol (1979) 1.12
Inheritance of Fuchs' endothelial dystrophy. Arch Ophthalmol (1971) 1.11
Blood groups in two Amish demes. Humangenetik (1967) 1.08
Familial nanophthalmos. Am J Ophthalmol (1976) 1.06
Ataxia-telangiectasia and Swiss-type agammaglobulinemia. Two genetic disorders of the immune mechanism in related Amish sibships. JAMA (1966) 1.02
Retinoblastoma in a patient with a 13qXp translocation. Am J Ophthalmol (1977) 1.00
A clinical and histopathological study of François-Neetens speckled corneal dystrophy. Am J Ophthalmol (1977) 0.99
Electrophysiologic properties of intercostal muscle fibers in human neuromuscular diseases. Muscle Nerve (1980) 0.96
Chronic myopathy induced by repeated bupivacaine injections. J Neurol Sci (1985) 0.94
Amish demography. Soc Biol (1970) 0.94
Axoplasmic flow in human sural nerve. Arch Neurol (1973) 0.92
Serial two-dimensional echocardiography in Duchenne muscular dystrophy. Neurology (1982) 0.91
Surgical treatment of dislocated lenses in the Marfan syndrome and homocystinuria. Trans Am Acad Ophthalmol Otolaryngol (1973) 0.91
Penetrance and variability in anterior chamber malformations. Birth Defects Orig Artic Ser (1979) 0.88
Genetic counseling of families with Best macular dystrophy. Trans Sect Ophthalmol Am Acad Ophthalmol Otolaryngol (1976) 0.87
Cancer of the cervix in an Amish population. Cancer (1968) 0.87
Verbal perseveration of dementia patients. Brain Lang (1985) 0.87
Duane's retraction syndrome and associated congenital malformations. Am J Ophthalmol (1972) 0.86
Alterations in lipid incorporation in Duchenne muscular dystrophy. Studies of fresh and cultured muscle. J Neurol Sci (1981) 0.86
Echocardiographic determination of contraction and relaxation measurements of the left ventricular wall in normal subjects and patients with muscular dystrophy. Circulation (1980) 0.84
Alterations in dopaminergic receptors in Huntington's disease. Life Sci (1977) 0.84
Bone formation at a ceramic implant interface. Calcif Tissue Res (1971) 0.83
Intercostal muscle biopsy in human neuromuscular disease. Histochemical and electron microscopic studies. J Neurol Neurosurg Psychiatry (1975) 0.83
Alterations in creatine kinase in fresh muscle and cell cultures in Duchenne dystrophy. Ann Neurol (1981) 0.82
Ultrastructural fiber typing in normal and diseased human muscle. J Neurol Sci (1975) 0.82
Hereditary proximal spinal and bulbar motor neuron disease of late onset. A report of six cases. Arch Neurol (1982) 0.81
Ocular trauma during amniocentesis. Arch Ophthalmol (1973) 0.80
Investigation of sounds produced by healthy and diseased human muscular contraction. IEEE Trans Biomed Eng (1986) 0.80
Behavior and histochemistry of functionally isolated cat ankle extensors. Exp Neurol (1973) 0.80
Conduction velocities in single fibers of diseased human muscle. Neurology (1979) 0.80
Acromegaly: histochemical and electron microscopic changes in deltoid and intercostal muscle. Neurology (1974) 0.79
Factors influencing osmotic fragility of red blood cells in Duchenne muscular dystrophy. Neurology (1980) 0.79
Altered polyamine excretion in Duchenne muscular dystrophy. Neurology (1981) 0.79
Drug trial of superoxide dismutase in Duchenne's muscular dystrophy. Arch Neurol (1982) 0.79
Observations on the innervation of human extraocular muscles. J Neurol Sci (1985) 0.79
Cell proliferation in response to vitreous hemoglobin. Invest Ophthalmol Vis Sci (1981) 0.79
Cerebrospinal fluid gamma-aminobutyric acid variations in neurological disorders. Arch Neurol (1977) 0.79
(Ca++ + Mg++)-ATPase of red cells in Duchenne and myotonic dystrophy: effect of soluble cytoplasmic activator. Neurology (1979) 0.78
Huntington's disease: regional alteration in muscarinic cholinergic receptor binding in human brain. Life Sci (1976) 0.78
Myopathy associated with sclerodermal facial hemiatrophy. Arch Neurol (1981) 0.78
Cancer of the cervix in the Amish. Trans Assoc Am Physicians (1967) 0.78
Serial left ventricular wall measurements in Duchenne's muscular dystrophy. J Am Coll Cardiol (1983) 0.77
Changes in end-plate cholinesterase and axons during muscle degeneration and regeneration. J Anat (1985) 0.77
Tornwaldt's disease. Onset as symptomatic (secondary) glossopharyngeal neuralgia. Neurology (1972) 0.77
Glass ceramic bone implants. J Biomed Mater Res (1972) 0.77
Polyamine metabolism in muscle: differential response to tenotomy and denervation in the soleus and gastrocnemius muscle of adult rats. Exp Neurol (1982) 0.77
Biochemical and histochemical evidence for stimulation of myosin ATPase activity in thyrotoxic rabbit heart. FEBS Lett (1977) 0.77
Language impairment in dementia. Ariz Med (1982) 0.77
Myopathy associated with linear scleroderma. A histochemical and electron microscopic study. Neurology (1975) 0.77
Altered muscle polyamine levels in human neuromuscular diseases. Ann Neurol (1981) 0.76
The fine structure of cortisone-induced myopathy. Exp Neurol (1972) 0.76
L-dopa in uremic patients with the restless legs syndrome. Int J Neurosci (1987) 0.76
A survey of neurological disorders in a genetic isolate. Neurology (1967) 0.75
External intercostal muscle biopsy. Arch Neurol (1975) 0.75
Inheritance in epidermolysis bullosa letalis. J Med Genet (1968) 0.75
Motor neuron disease: possible mechanisms of spontaneous electromyographic activity. Arch Phys Med Rehabil (1976) 0.75
Stimulatory effects of drugs for protein synthesis on muscle cell cultures in Duchenne dystrophy. Ann Neurol (1979) 0.75
The heritability of glaucoma. Trans Pac Coast Otoophthalmol Soc Annu Meet (1977) 0.75
Genetic counseling. Trans Am Acad Ophthalmol Otolaryngol (1973) 0.75
Myasthenia gravis. Ariz Med (1977) 0.75
Motor neuron disease: possible mechanisms of spontaneous electromyographic activity. Electromyogr Clin Neurophysiol (1978) 0.75
Alterations in brain muscarinic cholinergic receptor binding and choline acetyltransferase activity in Huntington's disease. Proc West Pharmacol Soc (1976) 0.75
Genetics for ophthalmologists. Trans Am Acad Ophthalmol Otolaryngol (1971) 0.75
Differential diagnosis and treatment of dislocated lenses. Birth Defects Orig Artic Ser (1976) 0.75
Factors influencing osmotic fragility of Duchenne red blood cells. Trans Am Neurol Assoc (1979) 0.75
Arcuate corneal opacities. Am J Med Sci (1977) 0.75
The heritability of strabismus. Am Orthopt J (1975) 0.75
[Not Available]. Hist Mex (1981) 0.75
Diphenylhydantoin reverses membrane effects in steroid myopathy. Nat New Biol (1972) 0.75
Editorial: The use and abuse of eponyms. Am J Ophthalmol (1973) 0.75
Elevated urinary polyamines in Duchenne muscular dystrophy. Trans Am Neurol Assoc (1979) 0.75
Histidinemia with features of the Marfan syndrome. J Pediatr (1975) 0.75
Mast syndrome: a recessively inherited form of presenile dementia with motor disturbances. Birth Defects Orig Artic Ser (1971) 0.75
Linkage studies of Best's macular dystrophy. Clin Genet (1988) 0.75
Ocular trauma during amniocentesis. N Engl J Med (1972) 0.75
Ectopia lentis in systemic heritable disorders. Birth Defects Orig Artic Ser (1974) 0.75
Myositis specific antibodies: frequency in different populations. Folia Neuropathol (2000) 0.75
Caffeine-modulated acetylcholine sensitivity in denervated rat and diseased human muscle. Life Sci (1975) 0.75
Familial agoitrous cretinism accompanied by musclar hypertrophy. Pediatrics (1968) 0.75
Corticosteroids. Effects on muscle membrane excitability. Arch Neurol (1972) 0.75
Recent advances in the neurochemistry of Huntington's disease. Ariz Med (1977) 0.75
Troyer syndrome: a recessively inherited form of spastic paraplegia with distal muscle wasting. Birth Defects Orig Artic Ser (1971) 0.75
The muscle spindle in cortisone-induced muscular atrophy. Exp Neurol (1973) 0.75
Diphenylhydantoin for steroid-induced muscle weakness. JAMA (1973) 0.75
Malignant hyperthermia. Ariz Med (1979) 0.75
Steroid myopathy. Ariz Med (1978) 0.75