Neudle.com: "kyphosis"

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal protrusion

accomodation, abnormal

Alzheimer's disease

anterior horn cell disease

arrhythmia, cardiac

asthma, poliomyelitis-like syndrome with

ataxia, truncal

atlanto-axial subluxation

basal ganglia, calcification of

basilar impression

benign essential tremor

bent spine syndrome

blinking, reduced

bone marrow transplantation

bulbar palsy, progressive

calcification, intracranial

CAT scan, abnormal

CAT scan, muscle

central core disease

cerebellar atrophy, primary

cerebellar vermis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrovascular accident

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chromosomal abnormality

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

codfish vertebrae

cogwheel rigidty

collagen vascular disease

contractures, joint

convergence, impaired

conversion reaction

cornea, abnormal

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

cranial nerve palsies

creatine phosphokinase(CPK)elevated

dermatoglyphics

developmental retardation

difficulty climbing stairs

diplegia, spastic cerebral

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

dropped head syndrome

dysostosis multiplex

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

facial anomalies

facial appearance, abnormal

facial hypoplasia

facial weakness

feeding disorder

flaccid paralysis

Friedreich's ataxia

frontal bossing

gait, festinating

genetic neurologic disorders

genetic testing

growth retardation

hemorrhage, intracranial, newborn

hepatosplenomegaly

heralding manifestation

histochemistry of muscle

hyperhomocysteinemia

hypotonia, infants

infection, recurrent

insulin resistance

intracranial hemorrhage

intrinsic hand muscles, wasting of

Isaacs syndrome

kinesia paradoxica

kyphoscoliosis, neurologic causes of

laryngeal spasm

leg weakness, bilateral

leg weakness, unilateral

lens, dislocation of

leukoencephalopathy

livedo reticularis

lysosomal storage disease

malignant hyperpyrexia

marche a petits pas

melanomatosis, primary malignant

mental retardation

metabolic disorder, primary

microspherophakia

mitral valve prolapse

monoclonal gammopathy

Morquio syndrome

motor neuron disease

movement disorder

movement disorder, extrapyramidal

mucopolysaccharidoses

muscle atrophy, progressive

muscle atrophy, static

muscle weakness

muscle weakness, proximal

muscular dystrophy

myasthenia gravis

myeloradiculopathy

myokymia, facial

myopathy, metabolic

nemaline rod myopathy

nemaline rod myopathy, adult onset

neurocutaneous disease

neuroichthyosis

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

night blindness

old age, neurology of

optic neuropathy

osteogenesis imperfecta

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinson disease, diagnosis

pathologic reflex

pectus carinatum

pectus excavatum

peroxisomal disease

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

poliomyelitis-like illness

postural abnormality

prenatal diagnosis by amniocentesis

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

Refsum's disease

respiratory failure

retinitis pigmentosa

root lesion, nerve

scoliosis, neurologic association with

sensorineural hearing loss

Sjogren-Larsson syndrome

skin, lesions in neurologic disorders

spastic diplegia

speech disorder

spinal cord, compression of

standing difficulty

stem cell transplantation

stooped posture

treatment of neurologic disorder

tremor, resting

visual fields, constricted

vocal cord paralysis

voice, abnormality of

weakness, progressive

weakness, proximal

white matter disease

Showing articles 0 to 21 of 21

A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016

Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

Camptocormia
Neurol 65:355-359, Azher,S.N. &Jankovic,J., 2005

Dropped Head Synd & Bent Spine Synd:Two Separate Clin Entities or Different Manifest of Axial Myopathy
JNNP 65:258-259, Oerlemans,W.G.H.&Visser,M., 1998

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

MRI of White Matter Changes in the Sjogren-Larsson Syndrome
Neuroradiology 37:576-577, Hussain,M.Z.&Aihara,M., 1996

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Poliomyelitis-Like paralysis During Recovery from Acute Bronchial Asthma:Possible Etiology and Risk Fators
Pediatrics 88:276-279, Shahar,E.M.,et al, 1991

Neurological Findings in Alzheimer's Disease and Normal Aging
Arch Neurol 47:625-627, Glasko,D.,et al, 1990

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Skeletel Fluorosis
In Vinken PJ, Bruyn GE, Ed, Handbook of Clin Neurol, Vol 36, North-Holland Publ Co, 465, Reddy,D.R., 1979

Isaac Syndrome with Laryngeal Involvement:An Unusual Presentation of Myokymia
Neurol 29:1612-1615, Jackson,D.L.,et al, 1979

Charcot-Marie-Tooth Disease Associated With"Essential Tremor"
Neurol Sciences 28:17-40, Salisachs,P.J., 1976

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

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

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

Showing articles 0 to 21 of 21