Neudle.com: "scoliosis neurologic association with"

Differential
(Click to cross reference)

abortion, spontaneous

acromicria

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Aicardi's syndrome

anesthesia, general

angiography, cerebral

angiography, spinal

angiokeratoma

anterior horn cell disease

anterocollis

anticoagulant, complications of

anticoagulant, treatment

apnea

areflexia

Arnold Chiari malformation

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, spinal

arthrogryposis multiplex

aspiration

asthma

asthma, poliomyelitis-like syndrome with

atlanto-axial subluxation

Babinski sign

basilar impression

benign essential tremor

bladder dysfunction

blindness

bone biopsy

bone marrow transplantation

botulinum toxin

brain atrophy

brainstem, hypoplasia

brainstem, malformation

Brown Sequard syndrome

cerebral palsy, associated problems with

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrovascular accident

cerebrovascular accident, young adult

cervical spine

cervical spine abnormality

Charcot-Marie-Tooth

children

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

Cobb syndrome

codfish vertebrae

cold hands sign

collagen vascular disease

coloboma

complications

compression fracture

congenital heart disease

congenital malformation

congenital myopathy

congestive heart failure

corpus callosum, atrophy of

corpus callosum, thinning

coumarin

cranio-cervical junction

creatine phosphokinase(CPK)elevated

developmental milestones, loss of

developmental retardation

differential diagnosis

dilantin

dimple

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dystonia, post traumatic

dystonia, treatment of

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

Emery-Dreifuss muscular dystrophy

encephalopathy

encephalopathy, progressive

eye movement, disorders of

face, elongated

facial anomalies

facial appearance, abnormal

facial hypoplasia

facial weakness

facial weakness, bilateral

foot ulcer, neuropathic

fourth ventricle, enlargement of

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

genetic neurologic disorders

hemorrhage, intracranial, newborn

heparin

hepatomegaly

hepatosplenomegaly

heralding manifestation

heterotopia

HGPPS

histochemistry of muscle

hypoxic encephalopathy

iatrogenic neurologic disorders

intellectual deterioration

intracranial hemorrhage

intrinsic hand muscles, wasting of

ipsilateral hemiplegia

Isaacs syndrome

joint hypermobility

kyphoscoliosis, neurologic causes of

leg weakness, bilateral

leg weakness, unilateral

lens, dislocation of

lens, ectopic

Lhermitte's sign

lid closure, weakness of

lysosomal storage disease

malformation, CNS, congenital

malignant hyperpyrexia

Marfan syndrome

medulla oblongata

medulla oblongata, lesion of

medulla oblongata, malformation

melanomatosis, primary malignant

menses

mental retardation

metabolic disorder, primary

mitral valve prolapse

MRI, diffusion tensor

MRI, diffusion weighted

MRI, muscle

mucopolysaccharidoses

multicore myopathy

multiminicore disease

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle pain

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, limb-girdle

myelogram

myelomeningocele

myelopathy

myelopathy, arteriovenous malfor.of spinal cord causing

neurologic complications

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination, non-focal

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

ocular motility, disorders of

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

optic atrophy

osteogenesis imperfecta

paraspinal muscle weakness

patient information and support

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

pneumonia

poliomyelitis

poliomyelitis-like illness

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prognathism

prognosis

progressive neurologic disorder

prolactin, elevated

pseudarthrosis

pseudohypertrophy

psychiatric problems in neurologic disorders

psychosis

ptosis

ptosis, bilateral

pulmonary function tests

pyramidal tract, uncrossed

rippling muscle disease

scoliosis, neurologic association with

screaming

screening

seizure

sensorineural hearing loss

sensory loss

short neck

short stature

skin, lesions in neurologic disorders

skull x-ray, abnormal

skull x-ray, bony defect on

SMN1 gene

somatosensory evoked potentials

spasticity

speech disorder

speech disorder, childhood

spinal cord, compression of

spinal cord, injury of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, vascular malformation of

spinal fusion

spinal muscular atrophy

spinal muscular atrophy, classification

spinal stenosis

spine, lesion of`

spinocerebellar ataxia

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subdural hematoma

subdural hematoma, neonates and infants

suboccipital decompression

tongue, fasciculations of

torticollis

torticollis, post traumatic

trauma

treatment of neurologic disorder

tremor

trinucleotide repeats

tyrosine hydroxylase deficiency

visual acuity, decreased

visual fields, constricted

weakness, progressive

x-ray, cervical spine

x-ray, lumbar spine

Showing articles 0 to 50 of 23025 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Clinical and Imaging Features of Cobb Syndrome
Neurol 102:e208118, Yang,X.,et al, 2024

Mortality and Causes of Death in Children with Cerebral Palsy with Scoliosis Treated with and without Surgery
Neurol 101:e1787-e1792, Ahonen,M.,et al, 2023

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

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

Degenerative Diseases of the Nervous System, Friedreich Ataxia
Adams & Victors Principles of Neurology, Chp 39, pg 1102, Ropper, A.H.,et al, 2014

Ipsilateral Stroke in a Patient with Horizontal Gaze Palsy with Progressive Scoliosis and a Subcortical Infarct
Stroke 42:e1-e3, Ng, A.S.L.,et al, 2011

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

Orthopedic Outcomes of Long-Term Daily Corticosteroid Treatment in Duchenne Muscular Dystrophy
Neurol 68:1607-1613, King,W.M.,et al, 2007

Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

Multiminicore Disease in a Family Susceptible to Malignant Hyperthermia: Histology, In Vitro Contracture Tests, and Genetic Characterization
Arch Neurol 61:106-113, Guis,S.,et al, 2004

Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000

Natural History of Scoliosis in Spastic Cerebral Palsy
Lancet 351:1687-1692, Saito,N.,et al, 1998

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993

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

Cervical Dystonia:Clinical Findings and Associated Movement Disorders
Neurol 41:1088-1091, Jankovic,J.,et al, 1991

Scoliosis:Spinal Cord Monitoring During Surgery
Lancet 338:219-220, , 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

The Effect of Spine Fusion on Respiratory Function in Duchenne Muscular Dystrophy
Neurol 41:38-40, Miller,R.G.,et al, 1991

Neurofibromatosis Type I in Children
J Pediatr 116:845-853, Listernick,R.&Charrow,J., 1990

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

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

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

Chiari Type I Malformation in Children
J Pediatr 115:573-576, Dure,L.S.,et al, 1989

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Practical Problems in the Respiratory Care of Patients with Muscular Dystrophy
NEJM 316:1197-1205, Smith,P.E.M.,et al, 1987

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

Tethered Cord Syndrome in Adults
J Neurosurg 57:32-47, Pang,D.&Wilberger,J.E.Jr., 1982

Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
Am J Med 68:122-140, Hall,J.G.,et al, 1980

Marfan Syndrome
NEJM 300:772-777, Pyeritz,R.E.,et al, 1979

The Aicardi Syndrome:Report of 4 Cases & Review of the Literature
Ann Neurol 5:475-482, Bertoni,J.M.,et al, 1979

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

Clinical Symposia, Scoliosis
CIBA, 30:21978., Keim,H.A., 1978

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

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

The Diagnosis & Natural History of Spinal Cord Arteriovenous Malformations
Mayo Clin Proc 51:637, Tobin,W.D.,et al, 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

Scoliosis
Neurologic Association with-Ciba Symposium, Vol 24, #1972., , 1972

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

Adverse Events Associated with Disease-Modifying Drugs for Multiple Sclerosis
Neurol 102:e208006, Ng, HS.,et al, 2024

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

Extensive Brainstem and Striatal Involvement in Neuropsychiatric Systemic Lupus Erythematosus
Neurol 102:e209153, Branch, A.,et al, 2024

Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024

A 30-Year-Old Woman Presenting with Rapidly Progressive Dementia and Extreme Hypoglycorrhachia
Neurol 102:e209188, Bai,X.,et al, 2024

Showing articles 0 to 50 of 23025 Next >>