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Differential
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areflexia
calf hypertrophy
creatine phosphokinase(CPK)elevated
diaphragmatic paralysis
distal muscle weakness
dyspnea
electromyogram
familial
gait disorder
gene mutation
hemidiaphragm, paralysis of
hereditary myopathy with early respiratory failure
inability to sit up
muscle weakness
myopathy
myopathy, hereditary
orthopnea
respiratory failure
steppage gait
titinopathy
vital capacity
weakness
weakness, progressive
Showing articles 750 to 800 of 4613 << Previous Next >>

Nerve Growth Factor (three parts)
NEJM 297:1096, 1149, 1211977., Mobley,W.C.,et al, 1977

Eosinophilic Polymyositis
Ann Neurol 1:65, Layzer,R.B.,et al, 1977

Clinical Pathological Conference
Multiple Myeloma with Paraneoplastic Motor Neuropathy & Cauda-equina Compression, Case Record 31-197, , NE97:266,1977., 1977

An unusual Cause of Apparent Epilepsy:ECG & EEG Findings in a Case of Jervell Lange-Neilson Syndrome
JNNP 40:1102, Selby,P.J.,et al, 1977

Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
Arch Neurol 34:567, Gilmartin,R.C.,et al, 1977

Upper Airway Obstruction in the Shy-Drager Syndrome
Ann Neurol 2:83, Israel,R.H., 1977

Acute Failure of Automatic Respirations Secondary to a Unilateral Brainstem Infarct
Ann Neurol 1:583, Levin,B.E.,et al, 1977

Pulmonary Hypertension & Sleep Apnea, (Letter)
NEJM 296:631, Ravin,C.E., 1977

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

Reversible Paralysis of Automatic Respiration in Multiple Sclerosis
Arch Neurol 34:686-689, Boor,J.W.,et al, 1977

Nerve-Growth Factor in Familial Dysautonomia
NEJM 295:671, Montalcini,R.L., 1976

Central Pontine Myelinolysis
Quart J Med 45:373, Tomlinson,B.E.,et al, 1976

Hypersomnia With Periodic Apneas in Acquired Micrognathia
Arch Neurol 33:769, Coccagna,G.,et al, 1976

Cause of Weakness in Myasthenia Gravis
NEJM 294:722, Grob,D., 1976

Clinical Use and Toxicity of Intravenous Lidocaine, A Report from the Boston Collaborative Drug Surveillance Program
Am Heart J 92:168-173, Pfeifer,H.J.,et al, 1976

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Posttraumatic Dysautonomic Cephalgia
Arch Neurol 32:649, Vijayan,N.,et al, 1975

Acute Areflexic Paralysis
Arch Neurol 32:706, Furlan,A.J.,et al, 1975

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Hepatic Encephalopathy:Current Status
Gastroenter 66:121:1974., Schenker,S.,et al, 1974

Neurologic Changes in Liver Disease
Brain Dysfunction in Metabolic Disorders, ed. by F. Plum, Res. Publ. Assn. Nerv. Ment. Dis. , Vol. 5, , New York:RaVictor, M., 1974

Defect in Automatic Respiration in a Case of Multiple Sclerosis
Am J Med 56:433-436, Rizvi,S.S.,et al, 1974

Hereditary Quadriceps Myopathy
JNNP 36:1041, Espir,M.L.E.,et al, 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Pathology of Malignant Hyperpyrexia
BMJ Editorial 249, 1973, Feb., , 1973

Neonatal Seizures
NEJM 289:413, Volpe,J., 1973

Impaired Peripheral Chemosensitivity & Acute Respiratiory Failure in Arnold-Chiari Malfor & Syringomyelia
NEJM 288:947, Bokinsky,G.E.,et al, 1973

Treating Problem Children with Stimulant Drugs
NEJM 289:407, Sroufe,L.A.,et al, 1973

Neurologic Manifestations of Progressive Systemic Sclerosis, 1972
Nebraska Med J 58:106, Aita,J.A., 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Lead Encephalopathy in Adults
Am J Med 52:289, Whitfield,C.L.,et al, 1972

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972

The Mucopolysaccharidoses
(Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971

Dominant Juvenile Optic Atrophy
Arch Ophthalmol 85:133, Caldwell,J.,et al, 1971

Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith
W. B. , Saunders Co. , 1970, 248-249., David,W., 1970

The Neuropathy of Acute Intermittent Porphyria
Quart J Med 38:307, 1969 July., Ridley,A., 1969

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

Myopathy of the Quadriceps Muscles
J Neurol Sci 7:201, VanWijngaarden,G.K.,et al, 1968

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Neurological Manifestations of Sarcoidosis
Neurol 15:1147, Wiederholt,W.,et al, 1965

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

Morquio's Disease, A Radiologic & Morphologic Study
Pediatrics 34:839-850, Schenk,E.A.&Haggerty,J., 1964

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Neurologic Manifestations of Chronic Pulmonary Insufficiency
NEJM 257:579-590, Austen,F.K.,et al, 1957

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025



Showing articles 750 to 800 of 4613 << Previous Next >>