Neudle.com: "hand posture"

Differential
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abdominal distention

abulia

accommodation

accomodation, abnormal

acetazolamide

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acrocyanosis

acromicria

acute ataxia of childhood

acute cerebellar ataxia

acute disseminated encephalomyelitis

Addison's disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

alexia without agraphia

algorithm

alien hand syndrome

alternating rapid movement

alternating rapid movement, impaired

amphiphysin antibodies

anemia, megaloblastic

anterior tibial muscle weakness

anticonvulsants, untoward effects of

antiviral agents

anxiety

aphasia

aphasia, progressive, primary

apraxia of eye movements

apraxia, constructional

aspartate aminotransferase

ataxia telangiectasia

ataxia, truncal, associated with ocular oscillations

attention deficit disorder with hyperactivity

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

behavior, combative

behavioral disorder

benign essential tremor

benzodiazepine

beta adrenergic blocker

bone marrow suppression

botulinum toxin

botulinum toxin, complications of

brain biopsy, stereotaxic

brainstem, dysfunction

brainstem, infarction of

calcification, intracranial

CAT scan, emission, abnormal

cauda equina, enhancement

CD4 counts

central cord syndrome

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral palsy

cerebral palsy, associated problems with

cerebral peduncle

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, complications with

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chromosomal abnormality

chromosome 14

chromosome 15

chromosome 6

chronic progressive external ophthalmoplegia

cirrhosis

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

concentration, impaired

convergence, impaired

conversion reaction

copper

copper metabolism, abnormal

cornea, abnormal

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cough

cranial nerve enhancement

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

cryptococcal meningitis

cryptorchidism

cultured skin fibroblasts

cytokines

cytomegalovirus infection

decerebrate posture

deep gray nuclei

degenerative cervical myelopathy

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

depression

dermatitis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty going down stairs

dilantin

dilantin, toxicity

diplopia

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

diurnal variation

dizziness

dopa responsive dystonia

dopamine antagonist

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze

drooling

drug abuse

drug abuse, inhalation

drug induced neurologic disorders

dysarthria

dysarthria-clumsy hand syndrome

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, focal lesion causing

dystonia, focal task specific

dystonia, laryngeal

dystonia, post traumatic

dystonia, psychogenic

dystonia, symptomatic

dystonia, treatment of

dystonic reaction, acute

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electrophoretic pattern, CSF

embolism

embolism, fat

encephalitis

encephalitis, acanthamoeba

encephalitis, amebic

encephalitis, autoimmune

encephalitis, episodic

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, St.Louis

encephalitis, viral

encephalomyelitis, paraneoplastic

encephalopathy

encephalopathy, parainfectious

encephalopathy, progressive

enzyme, defect

eosinophilia

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

executive dysfunction

exome sequencing

eye color

eye movement, disorders of

eyes, sunken

facial appearance, abnormal

facial expression abnormality

fetal movements, reduced

fetus

fever

fine motor function, impaired

finger naming

finger nose finger test

finger numbness

finger tapping

fingernails, abnormal

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, pathologic signs of

gammaglobulin therapy, intravenous

ganglionitis

gastric biopsy

gastritis

gastrocnemius muscle weakness

gastroenteritis

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genu of corpus callosum

gests antagoniste

Gilles de la Tourette syndrome

glabellar sign

globoid cells

globus pallidus

globus pallidus, lesion of

granular osmiphilic material

grasp reflex

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallervorden Spatz disease

hallucination

hallucination, visual

heavy metal intoxication

hemiakathisia

hemianopia

hemianopia, homonymous

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc

herniated disc, central

herniated disc, cervical

herniation syndromes, intracranial

hiccoughs

high arched feet

highly active antiretroviral therapy

hip flexor weakness

histochemistry

histochemistry of muscle

HIV CSF viral escape syndrome

human immunodeficiency virus type 1

human immunodeficiency virus type 1, asymptomatic

human immunodeficiency virus type 1, pathogenesis

hypopigmentation of skin

hyporeflexia

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

immunosuppressive agents

immunotherapy

impulsivity

inability to stand on tiptoes

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incoordination

industrial neurologic disorders

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intracranial pressure, increased

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaundice

jaw jerk, abnormal

Kayser-Fleischer ring

kinesia paradoxica

Krabbe's disease

lactic acidemia

lacunar infarction, differential diagnosis of

laminectomy

laminectomy, cervical

laminectomy, lumbar

language disorder in adults

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

lipid storage disorder of CNS

liver biopsy

liver disease

liver function enzymes

liver transplantation

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

medical-legal aspects of neurology

Mees lines

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis

meningoencephalitis

meningoencephalitis, amoebic

mental retardation

mental status, abnormal

merosin

metabolic disorder, primary-screening tests

methylmalonic acid, serum

methylmalonic acidemia

midbrain, infarction of

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

mimics

misdiagnosis

mitochondrial disease

molecular genetics

monoclonal gammopathy

mononeuropathy multiplex

mortality

motor dysfunction

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, psychogenic

movement disorder, treatment of

MPTP

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, hypointense signal foci on

MRI, negative

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRS

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, limb-girdle

musicians

musician's dystonia

myelinolysis, extrapontine

myelitis, longitudinal

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myositis, acute of childhood

myositis, post infectious

neoplasm, intracranial

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

nerve conduction studies, sensory

nerve root biopsy

neuritis, heavy metals causing

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neuroendocrinology

neurofibrillary degeneration

neuroleptic

neuroleptic malignant syndrome

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neuromuscular disease, electrodiagnosis of

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, chronic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

numb clumsy hands syndrome

numbness, extremity

numbness, generalized

nystagmus

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, vertical

obesity

occupational neurologic disorders

ocular motility, disorders of

Oculinum

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

opportunistic infection

opportunistic infection, CNS

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy

optic chiasm, enlarged

optic nerve, enlarged

optic neuropathy

ornithine transcarbamylase deficiency

orthostatic hypotension

osmotic demyelination syndrome

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

parasitic infection, CNS

paresthesias

paresthesias, feet

paresthesias, generalized

paresthesias, hands

parkin gene

Parkinson disease

Parkinson disease, asymmetric onset

Parkinson disease, axial symptoms

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, etiology of

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, heterogeneity of

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, mode of onset

Parkinson disease, prognosis of

Parkinson disease, psychogenic

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

paroxysmal nonkinesigenic dyskinesia

PAS positive

PAS positive material in the brain

past pointing

patient information and support

pelvic mass

penguin silhouette sign

penicillamine

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

photosensitivity, skin

pigmentary retinopathy

plasmacytoma

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleural effusion

POEMS syndrome

polymerase chain reaction

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyradiculoneuropathy

pons, lesion of

position sensation

position sensation, abnormal

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

posterior column disease

postoperative neurologic complications

postural abnormality

posturography

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

primary episodic ataxia

prion disease

prognosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

prolactin, elevated

propranolol

proprioception

proprioception, abnormal

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

pull test

pupil, dilated and fixed, bilateral

pure sensory stroke

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

rapid onset dystonia parkinsonism

rapidly fatal neurologic illness

rapidly progressing neurologic illness

rash

rash, hand

real-time quaking-induced conversion

Red flags

reflex sympathetic dystrophy

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

rheumatoid arthritis factor(R.A.factor)

rubella encephalitis, progressive

rubella virus

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis

schizophrenia

scoliosis

scoliosis, neurologic association with

screaming

screening

sea-blue histiocytes

sedimentation rate, elevated

seizure, psychomotor-temporal lobe

self harm

sensorineural hearing loss

sensory loss

sensory loss, asymmetric

sensory loss, cortical

sensory tricks

sequencing difficulty

seroconversion

serologic testing

serologic testing of cerebrospinal fluid

serum alanine aminotransferase

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

slurred speech

snout reflex

sodium valproate

sodium valproate, toxicity

speech disorder, childhood

speech disorder, non aphasic

speech, loss of

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinocerebellar ataxia type 3/Machado Joseph disease

splenomegaly

spontaneous remission

stem cell transplantation

stimulation, deep brain

stimulation, deep brain, bilateral

stooped posture

storage disease of CNS

strabismus

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

stuttering

subarachnoid hemorrhage

substantia nigra

suck reflex

suck, poor

superior cerebellar artery infarction

superior cerebellar artery syndrome

swallow evaluation

sweating

sweating, abnormality of

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

syphilis, ocular

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, protrusion of

tonic foot response

tonic spasms

torticollis

torticollis, post traumatic

toxoplasmosis, CNS

transcutaneous electrical nerve stimulation

transient ischemic attack

transient neurologic deficit

transient neurologic deficit, benign syndrome in young adults

trauma

treatment failure

treatment of neurologic disorder

tremor, post traumatic

trientine dihydrochloride

trinucleotide repeats

tripping

typing

typist cramp

tyrosine hydroxylase deficiency

uncal herniation

unconsciousness

unconsciousness, episodic

unconsciousness, transient

undiagnosed

upgaze, paralysis of

urea-cycle enzymopathies

uremia

uric acid, low

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

useless hand

uveitis

vascular endothelial growth factor

vegetarianism

ventricular enlargement

vertigo

vertigo, positional

vibratory sensation

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual symptoms

visuospatial disturbance

voice, abnormality of

walking

walking frame

walking, delayed

walking, difficulty with

weakness

weakness, congenital

weakness, generalized

weakness, progressive

weight loss

Wernekinck commissure syndrome

word-finding difficulty

Showing articles 0 to 50 of 1430 Next >>

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

Wernekinck Commissure Syndrome
Radiopaedia doi.org/10.53347/rlD-85274, Aug, Deng,F.,et al, 2023

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
Neurol 100:151-157, Horta,L.F.B.,et al, 2023

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
Cureus doi:10.7759/cureus 29225, Pelling,M.M., et al, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

A 68-Year-Old Man with Palmar Rash, Leg Pain, and Inability to Walk
Neurol 99:347-353, YoungHun, J.,et al, 2022

Clinical and Structural Findings in Patients with Lesion-Induced Dystonia
Neurol 99:e1957-e1967, Corp, D.T.,et al, 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

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

Clenched Fists as an Unusual Presentation of Focal Neuromyotonia
Neurol 97:e429-e430, Dhanapalaratnam, R.,et al, 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

A 65-Year-Old Woman with Tremor
Neurol 97:e1257-e1261, Ye, J.,et al, 2021

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Hand Posture as Localizing Sign in Adult Focal Epileptic Seizures
Ann Neurol 86:793-800, Ferando, I.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Degenerative Cervical Myelopathy
BMJ 360:k186, Davies, B.M.,et al, 2018

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,et al, 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

The Useless Hand of Oppenheim
Pract Neurol 17:464-468, Wiblin, L. & Guadagno, J., 2017

Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
NEJM 376:368-379, Case 3-2017, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

Orthostatic Tremor
Neurol 86:458-464, Hassan, A.,et al, 2016

50 Year Old Man with Cloudy Vision, Hearing Loss, and Unsteadiness
NEJM 374:2586-2593, Eliott, D.,et al, 2016

A 48-year-old Man with Walking Difficulty
Neurol 85:e165-e169, Kalladka, D.,et al, 2015

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
Adams & Victors Principles of Neurology, Chp 37, pg 968, Ropper, A.H.,et al, 2014

The Treatment of Dystonic Tremor: A Systematic Review
JNNP 85:759-769, Fasano, A.,et al, 2014

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,et al, 2014

Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Dystonia Musculorum Deformans
Adams & Victors Principles of Neurology, Chp 39, pg 1099, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Cerebellar Degeneration
Adams & Victors Principles of Neurology, Chp 39, pg 1105, Ropper, A.H.,et al, 2014

A Man with Tingling Fingers
BMJ 346:f1443, Larkman, M.,et al, 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Parkin Disease
JAMA Neurol 70:571-579, Doherty, K.,et al, 2013

Showing articles 0 to 50 of 1430 Next >>