Neudle.com: neuropathy sensory hereditary

Differential
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abducens nerve paralysis

acoustic nerve

acral sensory symptoms

Addison's disease

Adies pupil

adrenoleukodystrophy

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol

alcohol intolerance

alcoholic polyneuropathy

alkylating agents

altered states of consciousness

alternating rapid movement

amitriptyline

amyloid

amyloid angiopathy, cerebral

amyloidosis

amyloidosis, oculoleptomeningeal, familial

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

ankle reflex, absent

anterior interosseous neuropathy

anterior tibial muscle weakness

arthrogryposis multiplex

arthropathy

arthropathy, neuropathic

auditory evoked brainstem potentials

autonomic dysfunction

autonomic nervous system

autonomic neuropathy

autonomic neuropathy, idiopathic

B 12 deficiency

Babinski sign

bacterial infection

Bassen-Kornzweig syndrome

benign essential tremor

blacks

bladder dysfunction

blindness

blood dyscrasias, neurologic findings with

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial neuritis, prognosis of

brachial plexus

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

CAT scan, metrizamide

CAT scan, myelogram with

cataracts

cataracts, congenital

cauda equina

cauda equina, enhancement

cauda equina, lesion of

cavernous sinus

cavernous sinus, lesion of

central core disease

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, secondary

cerebellar lesion

cerebellum, disease of

cerebro hepato renal syndrome

cerebrospinal fluid, pressure low

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chromosomal abnormality

chromosome 16

chromosome 17

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

cold temperature

coloboma

compression neuropathy

compression neuropathy, recurrent

cornea, abnormal

cornea, opacity of

corpus callosum, lesion of

cough

cranial nerve enhancement

cranial nerve enlargement

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

deafness

degenerative diseases of CNS

Dejerine-Sottas syndrome

dementia

demyelinating disease

denervation of muscle

dermatomyositis

diabetes mellitus

diarrhea

differential diagnosis

diplegia, brachial

diplopia

diplopia, transient

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

DNA probes

down-beat nystagmus

drug induced neurologic disorders

electrocardiogram, abnormal

electroencephalogram, inflammatory disease

electromyogram

electronystagmography

electroretinograph

encephalopathy

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

erythromelalgia

evoked potentials

eye movement, disorders of

face, numbness of

facial nerve palsy, bilateral

facial pain

facial weakness

facial weakness, bilateral

Fazio-Londe's disease

fever

fibrillations

fine motor function, impaired

fundus, abnormality of

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

genu of corpus callosum

giant axonal neuropathy

Guillain Barre syndrome

hair analysis

Hallervorden Spatz disease

heavy metal intoxication

heel-knee-shin test

hemiparesis

hemiparesis, transient

human immunodeficiency virus type 1

idiopathic polyneuropathy

imbalance

impotence

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

incoordination

intellectual deficit

internuclear ophthalmoplegia

intracerebral hemorrhage

intracerebral hemorrhage, familial

intrinsic hand muscles, wasting of

Kearns-Sayre syndrome

keratitis

klippel feil syndrome

Korsakoff's psychosis

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

kyphosis

laminectomy, cervical

laminectomy, lumbar

Laurence-Moon-Bardet-Biedl syndrome

Leber's congenital amaurosis

leg weakness, bilateral

leprosy

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

leukopenia

light-near dissociation, causes of

liver transplantation

lumbosacral plexopathy

magnetic stimulation, brain

median neuropathy

meningismus

meningoencephalopathy

mental retardation

methotrexate

methylhydrazine derivatives

methylmalonic acid, serum

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

misdiagnosis

mitochondrial disease

molecular genetics

monoamine oxidase inhibitors

monoclonal gammopathy

mononeuropathy

mononeuropathy multiplex

mononeuropathy, children

mononeuropathy, recurrent

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, peripheral nerve

MRI, spinal cord

MRI, spine

mucopolysaccharidoses

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle weakness

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, familial incidence of

myasthenia gravis, nystagmus in

myasthenia gravis, ocular

myasthenia gravis, sensory loss with

myasthenic crisis

myelin protein zero gene

myopathy, carcinomatous

myopathy, mitochondrial

myopathy, thyroid disease causing

nerve biopsy, indication

nerve conduction studies

nerve conduction studies, sensory

nerve growth factor

nerve growth stimulating activity

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuritis, causes of

neuroblastoma

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, burden

neurologic disease, diagnoses of

neuromuscular disease, electrodiagnosis of

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronopathy

neuronopathy, sensory

neuropathy

neuropathy, amyloid

neuropathy, ataxic

neuropathy, classification of

neuropathy, demyelinating

neuropathy, diabetic

neuropathy, etiologies of

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, onion bulb

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, recurrent

neuropathy, sensory

neuropathy, sensory, hereditary

neuropathy, work up for

neurotoxin

neurotrophin-3

next-generation sequencing

night blindness

nitrogen mustard

numbness, extremity

nutritional deficiency

nystagmus

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, monocular

optic atrophy

optic atrophy, hereditary

optic nerve

optic neuropathy

orthostatic hypotension

orthostatic hypotension, idiopathic

paraparesis, familial spastic

paraparesis, spastic

paresthesias

paresthesias, feet

paresthesias, lower extremity

patient information and support

peroneal muscle atrophy, causes of

peroneal nerve

peroneal nerve, lesion of

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

POLG1 gene

poliomyelitis

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic idiopathic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic relapsing

polyneuropathy, familial

porphyria

positional head-hanging test

positive sharp waves

post polio syndrome

precipitating factors

pregnancy, neurologic complications in

procarbazine

prognosis

progressive neurologic disorder

proptosis

proximal muscle atrophy

pseudointernuclear ophthalmoplegia

psychological testing

pulmonary function tests

pupil

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, scalloped

pyramidal

pyramidal tract dysfunction

pyridoxine deficiency

quadriparesis

quadriplegia, transient

quality of life

radial nerve, palsy of

radiculopathy

reading disorder, acquired

reversible neurologic disorder

saccadic eye movements, abnormal

sarcoidosis

scoliosis

seizure

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss

sensory loss, leg

sensory loss, truncal

sensory nerve action potentials

sensory polyneuropathy

skin, lesions in neurologic disorders

somatosensory evoked potentials

spasticity

speech disorder

speech disorder, non aphasic

spinal cord, compression of

spinal muscular atrophy

spinal stenosis

spinal stenosis, familial

spinocerebellar ataxia

spinocerebellar degeneration

splenium of corpus callosum

splenomegaly

spontaneous muscle activity

spontaneous remission

steppage gait

steroid therapy, CNS treatment and complications with

suprascapular neuropathy

symmetric brain lesions

syncope

tandem gait, ataxic

Tangier's disease

tapetoretinal degeneration

tauopathy

tensilon test

thalamus, lesion of

thalamus, lesion of-bilateral

tomaculous neuropathy

tongue, enlarged

torticollis

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tricresylphosphate

trigeminal nerve

trigeminal nerve, hypertrophy

trigeminal neuralgia

trinucleotide repeats

ulnar neuropathy

ultrasonography, nerve

urinary incontinence

Usher's syndrome

vestibular areflexia

vestibular function, tests of

vestibulopathy

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

viral infection

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, congenital

vitreous opacities

vocal cord paralysis

voice, abnormality of

walking frame

walking, difficulty with

walking, difficulty with in dark

weakness

weakness, generalized

weakness, progressive

weakness, proximal

weight loss

Werdnig-Hoffman disease

Showing articles 600 to 650 of 5349 << Previous Next >>

Mononeuritis Multiplex in Polyarteritis Nodosa
Neurol 14:434, Lovelace,R.E., 1964

Intracranial Aneurysms Causing Ophthalmoplegia
Arch Ophthal 70:75l, Cogan,D.,et al, 1963

Syndrome of the Numb Chin
Arch Int Med 112:819-821, Calverley,J.F.,et al, 1963

Anatomic Pathways Related to Pain in Face & Neck
J Neurosurg 19:116, Taren,J.,et al, 1962

Anaesthesia of the Lower Lip
Br Dent Jour 113:423, Seward,M.H.E., 1962

Isolated Trigeminal Neuropathy-A Report of 16 Cases
Brain 82:391, Spillane,J.,et al, 1959

An Unusual Variant of Acute Idiopathic Polyneuritis (Syndrome of Ophthalmoplegia, Ataxia, & Areflexia)
NEJM 255:57, Fisher,C.M., 1956

Ischaemic Sensory Loss in Patients with Peripheral Nerve Lesions
JNNP 17:104, Gilliatt,R.W.,et al, 1954

Neuritis Produced by a Wristlet Watch
Lancet 1:993, Stopford,J.S.B., 1922

Cerebellar Ataxia in Children
Handout & References., Gilbert,J.J., 1850

Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
Stroke 57:148-156, Mania-Paris,L.,et al, 2026

Clinicopathologic Conference, Lyme Neuroborreliosis and Coinfection with Babesia Microti
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Neurosyphilis with Abnormal in the Bilateral Pons and Multifocal Cranial Nerve Enhancement
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Niemann-Pick Type C Disease
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Bilateral Posterior Limb Internal Capsule T2 Hyperintensity and Severe Cerebellar Atrophy in 2 Lifelong Friends
Neurol 106:e218014, Inoue,H.,et al, 2026

Glucagon-like Peptide-1 Receptor Agonists and Risk of Nonarteritic Anterior Ischemic Optic Neuropathy
Neurol 106:e214864, Dhivagaran,T.,et al, 2026

A 32-Year-Old Woman with Progressive Vision Loss and Confusion
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A 35-Year-Old Man with Recurrent Asymmetric Lumbosacral and Cervical Plexopathy
Neurol 106:e214910, Tayade,K.S., et al, 2026

Frequency of AQP4 and MOG Antibodies in Patients with Optic Neuritis Fulfilling Minimal New Multiple Sclerosis MRI Criteria
Neurol 106:e214753, Deschamps,R.,et al, 2026

Ribbon-Like Sign in Convexity Subarachnoid Hemorrhage
Ann Neurol 99:881-882, Liu,S-X.,et al, 2026

Trident Sign in GFAP-Associated Meningoencephalomyelitis
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Melas Syndrome
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Diagnosis of Multiple Sclerosis: 2024 Revisions of the McDonald Criteria
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A 66-Year-Old Man with Chronic Orthostatic Hypotension
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A 62-Year-Old Man with Symmetric Saddle Hypoesthesia and Sphincter Dysfunction
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Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
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Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
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A 64-Year-Old Man with Confusion, Nausea, Seizure, and Fever
Neurol 104:e213659, Xu,A.,et al, 2025

Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
Neurol 104: e213682, Hayakawa,I.,et al, 2025

Multivessel Cerebral Occlusion in Noonan Syndrome
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Neurosyphilis
Ann Neurol 98:1070-1076, Minter,D.J. & Chow,F.C., 2025

A 24-Year-Old Man With Persistent Spontaneous Dizziness
Neurol 105:e214337, Isaza-Pierotti,D.F., et al, 2025

Acromegaly
NEJM 393:1926-1939, Giustina,A. & Colao,A.,, 2025

An 83-Year-Old Female Patient with a Pupil Involving Oculomotor Nerve Palsy
Neurol 105:e214383, Riegel,D.C.,et al, 2025

Neuropathologic Changes in People with Essential Tremor With Dementia
Neurol 105:e214310, Wainman,E.,et al, 2025

A 16-Year-Old Adolescent Boy with Ophthalmoplegia and Unilateral Ptosis
Neurol 105:e214430, Lu,Y.,, 2025

A 30-Year-Old Female Patient with Multiple Sclerosis Presenting with Rapidly Progressive Cranial Neuropathies, Weakness, and Ataxia
Neurol 105:e214429, Trentadue,T.,et al, 2025

Clinicopathologic Conference, Diffuse Meningeal Melanomatosis
NEJM 393:2152-2162, Case 34-2025, 2025

Clinicopathological Conference, Powasan Virus Encephalitis
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AAV9-Mediated Gene Therapy for Infantile-Onset Pompes Disease
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A 27-Year-Old Man with Progressive Bilateral Vision Loss Resistant to Steroid Therapy
Neurol 105: e213897, Zhang,W.,et al, 2025

The Spectrum of Fragile X Disorders
NEJM 393:281-288, Hagerman,R.H. & Hagerman,P.J., 2025

Pan-Neurofascin Nodo-Paranodopathy Presenting as Fulminant Guillain-Barre Syndrome
Neurol 105:e213848, Cabral,A.,et al, 2025

GLP-1RA-Associated Diabetic Lumbosacral Radiculoplexus and Common Fibular Neuropathies
Neurol 105:e213916, Triplett,J.D.,et al, 2025

A 2-Year-Old Girl with Acute Encephalopathy After Febrile Systemic Illness
Neurol 105:e213970, Westendfortp,W.F.,et al, 2025

Pneumocephalus Leading to Basilar Artery Compression After Epidural Anesthesia
Neurol 105:e214089, Schick,J.,et al, 2025

A 72-Year-Old Man with Progressive Pan-Dysautonomia
Neurol 105:e213994, Zelikovich,A.S.,et al, 2025

A 9-Year-Old Girl with CNS Immune Dysregulation
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Infantile Epileptic Spasms Syndrome (West Syndrome)
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A 73-Year-Old Man With Progressive Proximal Muscle Weakness and Binocular Diplopia
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Showing articles 600 to 650 of 5349 << Previous Next >>