Neudle.com: "toe walking"

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Differential
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acral sensory symptoms

advances in neurology

anesthesia, general

ankle reflex, absent

anterior tibial muscle weakness

anticardiolipin antibodies

antiphospholipid antibody syndrome

antiviral agents

arrhythmia, cardiac

ataxia, cerebellar

ataxia, progressive

atherosclerosis, generalized

atrial fibrillation

atrial paralysis

atrioventricular block

attention deficit disorder with hyperactivity

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

biopterin deficiency

blue toe syndrome

burning paresthesia

calf hypertrophy

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebral embolism

cerebral embolism, carotid origin

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, young adult

cerebrovascular disease, surgical treatment of

Charcot-Marie-Tooth

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cogwheel rigidty

collagen vascular disease

congestive heart failure

contractures, joint

corpus callosum, lesion of

corpus callosum, thinning

creatine phosphokinase(CPK)elevated

developmental disability

developmental milestones, loss of

dexterity, impaired

diabetes mellitus

differential diagnosis

difficulty going down stairs

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

dystonia, treatment of

electrocardiogram, abnormal

electroencephalogram, inflammatory disease

embolism, aortic

embolism, atheromatous

embolism, cholesterol

embolism, platelet

Emery-Dreifuss muscular dystrophy

endarterectomy, carotid

endocarditis, neurologic manifestations with

epileptic encephalopathy

exome sequencing

failure to thrive

FARS2 deficiency

fine motor function, impaired

finger nose finger test

foot ulcer, neuropathic

Friedreich's ataxia

genetic counselling

genetic neurologic disorders

genetic testing

Gowers maneuver

growth retardation

heart block, complete

hematuria, microscopic

high arched feet

implantable cardioverter defibrillator

influenza A virus

influenza B virus

intrinsic hand muscles, wasting of

Krabbe's disease

leg weakness, bilateral

life expectancy

lysosomal storage disease

malignant hyperpyrexia

meningitis, CSF cell count-normal

mental retardation

microangiopathy, brain

microvascular thrombi

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

molecular genetics

movement disorder

muscle atrophy, progressive

muscle tenderness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, limb-girdle

myelin protein zero gene

myopathy, myofibrillar

myopathy, quadriceps

myositis, acute of childhood

myositis, post infectious

myotonic discharges

nerve conduction studies

nerve hypertrophy

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neuronopathy, sensory

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

next-generation sequencing

night blindness

numbness, extremity

nystagmus, gaze-evoked

orthostatic hypotension

pacemaker, cardiac-transvenous

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

Parkinson disease, differential diagnosis of

Parkinson disease, juvenile

Parkinsonism syndrome

periarteritis nodosa

peripheral vascular disease

pons, lesion of

positive sharp waves

progressive neurologic disorder

proximal muscle atrophy

pupil, dilated and fixed, bilateral

pyramidal tract dysfunction

respiratory failure

rippling muscle disease

seizure, children

shoulder, pain in

spastic diplegia

spinocerebellar ataxia

steroid therapy, CNS treatment and complications with

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

thrombotic thrombocytopenia purpura

transient ischemic attack

treatment of neurologic disorder

tremor, intention

tremor, postural

trinucleotide repeats

urea-cycle enzymopathies

viral infection

visual impairment

walking, delayed

walking, difficulty with

weakness, progressive

weakness, proximal

white matter disease

wide based gait

winging of scapula

Showing articles 0 to 24 of 24

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

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

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

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

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

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Overview of Acute Arterial Occlusion of the Extremities (Acute Limb Ischemia)
UptoDate Aug, Mitchell, M.E. & Carpenter, J.P., 2017

Approach to the Differential Diagnosis of Leg Ulcers
UptoDate Aug, Petersen, M.J., 2017

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,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, Hereditary Spastic Paraplagia
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias
Neurol 74:775-778, Karam,C. &Scelsa,S., 2010

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

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Benign Acute Childhood Myositis, Laboratory and Clinical Features
Neurol 53:2127-2131, Mackay,M.T.,et al, 1999

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Arginase Deficiency Presenting as Cerebral Palsy
Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Atherothrombotic Microembolism of Lower Ext (Blue Toe Synd) from Atheroscler Non-Aneurysmal Aortic Plaques
J Cardiovasc Surg 31:87-91, Benvegna,S.,et al, 1990

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Case Record of MGH-NEJM Atheromatous Emboli to Brain
Kidney, 286:11461972., , 1972

Showing articles 0 to 24 of 24