Neudle.com: "clumsy hand"

Differential
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abscess, vertebral

abulia

acetazolamide

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

acrocyanosis

acute disseminated encephalomyelitis

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

agenesis of corpus callosum

alexia without agraphia

alien hand syndrome

alpha-synuclein

alternating rapid movement

alternating rapid movement, impaired

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis-like syndrome

ANA

anatomy of

anemia

anemia, megaloblastic

anesthesia, general

ankle reflex, absent

anorexia

anterior horn cell disease

anti citrullinated antibody

anti IgLON5

anti Tr antibodies

anticonvulsants

anticonvulsants, untoward effects of

antithyroid antibodies

apraxia of eye movements

apraxia, constructional

ataxia telangiectasia

atrioventricular block

attention deficit disorder with hyperactivity

attention span

atypical

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune cerebellar ataxia

autoimmune disease

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Bell's phenomenon

benign essential tremor

benign essential tremor, refractory

bone marrow transplantation

brachial neuritis

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain biopsy, stereotaxic

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

carbamazepine, toxicity

CAT scan, emission, abnormal

CAT scan, myelogram with

CAT scan, ring sign

cataplexy

central cord syndrome

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar infarction

cerebellar lesion

cerebellum

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral dominance

cerebral embolism

cerebral embolism, cardiac origin

cerebral hemisphere left-right asymmetry

cerebral palsy

cerebral palsy, associated problems with

cerebral peduncle

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrovascular accident

Chediak-Higashi syndrome

children

chorea

chromosomal abnormality

chromosome 17

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

concentration, impaired

conduction block

confusion

congenital ocular motor apraxia

congestive heart failure

consanguinity

contractures, joint

convergence, impaired

cornea, opacity of

corona radiata

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cough

cranial neuropathy

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

degenerative cervical myelopathy

degenerative diseases of CNS

delay in diagnosis

delayed muscle relaxation

dementia

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

depression

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

digiti quinti sign

diplegia, brachial

diplopia

disability, neurological

disc space infection

disc space narrowing

discitis

disconnection syndrome

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dizziness

dopamine agonist

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze

drawing test in children

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, cervical

dystrophin

electroencephalogram, abnormalities of

electromyogram

electrophoretic pattern, CSF

embolism

Emery-Dreifuss muscular dystrophy

empyema, epidural-spinal

encephalitis

encephalitis, autoimmune

encephalopathy

enzyme, defect

enzyme, serum

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

episodic unconsciousness

evoked potentials

eye color

eye movement, disorders of

failed medical management

failure to thrive

falling

familial

familial periodic ataxia

FARS2 deficiency

fasciculation

fatigue

fatty acid, elevated plasma content

fetal tissue

fever

fibrillations

fine motor function, impaired

finger naming

finger nose finger test

Friedreich's ataxia, late onset

frontal lobe, pathologic signs of

gadolinium

gait disorder

gait, apraxic

gammaglobulin therapy, intravenous

ganglionitis

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

glabellar sign

Gowers maneuver

granular osmiphilic material

heart block, complete

hemianopia, homonymous

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herniated disc

herniated disc, central

herniated disc, cervical

human immunodeficiency virus type 1

hyperpigmentation of skin

iatrogenic neurologic disorders

immunosuppressive agents

immunotherapy

inattention

inborn errors of metabolism

inclusion bodies, intracytopasmic

incoordination

industrial neurologic disorders

infant, evaluation of

inferior olivary nucleus

insomnia

intellectual deficit

intellectual deterioration

intelligence quotient

internal capsule

intrathecal medication

intrauterine

intrinsic hand muscles, wasting of

introverted

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaundice

Kayser-Fleischer ring

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, differential diagnosis of

laminectomy

laminectomy, cervical

language disorder in adults

lateropulsion

L-dopa

learning disability

learning disability, in children

leg numbness

leg weakness, bilateral

leukocyte peroxidase

leukodystrophy

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukopenia

Lewy body

Lhermitte's sign

lipid storage disorder of CNS

liver disease

liver function enzymes

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macrocephaly

masked facies

medulla oblongata, neoplasm of

megalencephaly

megalencephaly, idiopathic

memory, defect of recent

memory, impairment of

meningitis

meningitis, bacterial

meningitis, children

meningitis, CSF cell count-normal

meningitis, factors influencing mortality in

meningitis, late neurologic sequelae in

meningitis, neurologic aspects and complications of

mental retardation

mental status, abnormal

metabolic disorder, primary-screening tests

methanol intoxication

methylmalonic acid, serum

methylmalonic acidemia

microcephaly

midbrain

midbrain, atrophy

midbrain, infarction of

migraine

miosis

misdiagnosis

mitochondrial disease

motor neuron disease, misdiagnosis

motor symptoms

motor system

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

mucopolysaccharidoses

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle spasm

muscle spasm, paraspinal

muscle stiffness

muscle twitching

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

musicians

myelitis

myelitis, longitudinal

myelopathy, chronic progressive

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve hypertrophy

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular disease, electrodiagnosis of

neuromyotonia

neuromyotonia and axonal neuropathy

neuronal ceroid-lipofuscinosis

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, sensory

neuropathy, toxic

neurotoxic

next-generation sequencing

Niemann-Pick disease

nitrous oxide

numb clumsy hands syndrome

numbness, extremity

nystagmus

nystagmus, vertical

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

olivary degeneration, hypertrophic

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection, CNS

optic atrophy

optokinetic nystagmus, abnormal

ornithine transcarbamylase deficiency

osteomyelitis

osteomyelitis, spinal

overuse syndrome

pacemaker, cardiac-transvenous

paraparesis, familial spastic

paresthesias, generalized

paresthesias, hands

parietal lobe, lesion of

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, diagnosis

Parkinson disease, nonmotor problems of

Parkinson disease, pathogenesis of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism syndrome

past pointing

pathologic reflex

penguin silhouette sign

peripheral blood smear, abnormal

Poretti-Boltshauser syndrome

position sensation

positional head-hanging test

positive sharp waves

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

posterior column disease

posterior fossa

posterior fossa, lesion of

postural abnormality

precipitating factors

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

prenatal

prevention of neurologic disorders

primary episodic ataxia

prion disease

prion protein gene

prognosis

progressive ataxia and palatal tremor

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

propranolol

proprioception

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

pupil

pupil, light reflex, abnormal

pure dysarthria

pure motor hemiplegia

pure sensory stroke

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal

pyramidal tract dysfunction

quadriparesis

radiculopathy

rapidly progressing neurologic illness

rash

reading disorder, acquired

real-time quaking-induced conversion

recruitment

recruitment, reduced

recurrent

reflex sympathetic dystrophy

reflex, cutaneous

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal failure

respiratory tract infection

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rubella encephalitis, progressive

rubella virus

saccadic eye movements, abnormal

safety

scoliosis

sedimentation rate, elevated

seizure

seizure, children

seizure, drug-induced

seizure, laughing as manifestation

seizure, treatment of, polytherapy

self harm

sensorimotor stroke

sensorineural hearing loss

sensory loss

sensory loss, asymmetric

sensory loss, cortical

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

skin, lesions in neurologic disorders

skin, temperature difference

sleep pathology and physiology

slit lamp examination

slurred speech

snout reflex

sodium valproate

sodium valproate, toxicity

somatosensory evoked potentials

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

spelling

spinal cord

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar degeneration

splenomegaly

spontaneous remission

square wave jerks

staggering

startle myoclonus

stem cell transplantation

steppage gait

stimulation, deep brain

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

suck reflex

sudden death

superior cerebellar artery infarction

superior cerebellar artery syndrome

symmetric brain lesions

thalamus, focused ultrasound ablation

thalamus, infarction of

thalamus, lesion of-bilateral

thyroiditis

titubation

toe walking

tone, muscle, increased

tongue, enlarged

tongue, smooth

tongue, swelling

transient ischemic attack

transient neurologic deficit

transient neurologic deficit, benign syndrome in young adults

treatment of neurologic disorder

tremor, surgical treatment of

tremor, treatment of

trinucleotide repeats

tripping

unconsciousness

unconsciousness, episodic

unconsciousness, transient

undiagnosed

upgaze

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

very long chain fatty acids

vestibulopathy

vibratory sensation

vibratory sensation, abnormal

visuospatial disturbance

voice, abnormality of

walking frame

walking, difficulty with

weakness

weakness, progressive

weight loss

Wernekinck commissure syndrome

word-finding difficulty

workup

writing

Showing articles 0 to 50 of 833 Next >>

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

Wernekinck Commissure Syndrome
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

A 6-Year-Old Boy with Muscle Twitching
Neurol 96:e301-e304, Lewis, H.S.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

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

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

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

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

A 60-year-old man with arm weakness and numbness
Neurol 90:190-196, Foster, L.A.,et al, 2018

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

Essential Tremor
NEJM 378:1802-1810, Haubenberger, D.,et al, 2018

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

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

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

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 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

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

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

Motor Neurone Disease
BMJ 349:g4052, Nageshwaran, S.,et al, 2014

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

Degenerative Diseases of the Nervous System, Friedreich Ataxia
Adams & Victors Principles of Neurology, Chp 39, pg 1102, 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

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

Early Child Development and Exposure to Antiepileptic Drugs Prenatally and Through Breastfeeding
JAMA Neurol 70:1367-1374, Veiby, G.,et al, 2013

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

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
JNNP 83:159-163, Guettard,E.,et al, 2012

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
NEJM 364:1856-1865, Case 14-2011, 2011

Validation of the Coin Rotation Test: A Simple, Inexpensive, and Convenient Screening Tool for Impaired Psychomotor Processing Speed
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Parkinsons Disease
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Motor Development in Very Preterm and Very Low-Birth-Weight Children From Birth to Adolescence: A Meta-Analysis
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Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Clinicopath Conf., Multifocal Motor Neuropathy With Conduction Block
NEJM 357: 2707-2715, Case 40-2007, 2007

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Clinical Study of 35 Patients with Dysarthria-Clumsy Hand Syndrome
JNNP 75:231-234, Arboix,A.,et al, 2004

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

Clinicopath Conf., Acute Disseminated Encephalomyelitis
NEJM 347:1433-1440, Case 34-2002, 2002

Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
JNNP 71:81-87, Selim, M. and Drachman, D.A., 2001

Clumsiness, Confusion, Coma, and Valproate
Lancet 353:1408, Ellaway,C.J.,et al, 1999

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Showing articles 0 to 50 of 833 Next >>