Neudle.com: high arched feet

Differential
(Click to cross reference)

abdominal distention

adult polyglucosan body disease

adverse drug reaction

airway obstruction

anemia

anemia, megaloblastic

anorexia

anosmia

anterior tibial muscle weakness

arthrogryposis multiplex

attention deficit disorder with hyperactivity

autonomic dysfunction

autonomic neuropathy

autonomic neuropathy, idiopathic

B 12 deficiency

Babinski sign

BAL

basophilic stippling of red blood cells

benign essential tremor

blood dyscrasias, neurologic findings with

bone marrow suppression

cataracts, congenital

central core disease

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

Charcot-Marie-Tooth

children

chromosomal abnormality

chromosome 17

chromosome 9

complete blood count

congenital bilateral perisylvian syndrome

congenital malformation

congenital myasthenic syndromes

corpus callosum, lesion of

corpus callosum, thinning

creatine phosphokinase(CPK)elevated

deafness

deep tendon reflexes

dermatitis

developmental abnormality of brain

developmental disability

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, ocular complications in

diabetic cranialneuropathies

diarrhea

differential diagnosis

difficulty going down stairs

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

drooling

dysarthria

dyskinesia, buccal lingual facial

dysmorphic

dysphagia

edema, pedal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

facial weakness, bilateral

falling

familial

fatigue

fine motor function, impaired

fingernails, abnormal

gag reflex, depressed

genetic neurologic disorders

genetic testing

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

heavy metal intoxication

hemoglobinuria

hepatitis

heralding manifestation

high altitude sickness

hypogonadism, hypogonadotropic

intrinsic hand muscles, wasting of

kyphoscoliosis, neurologic causes of

kyphosis

leg weakness, bilateral

leukodystrophy

leukopenia

light-near dissociation, causes of

liver disease

liver function enzymes

lordosis

lysosomal storage disease

malformation, CNS, congenital

malignant hyperpyrexia

Mees lines

memory, defect of recent

memory, impairment of

mental retardation

mestinon

methylmalonic acid, serum

methylmalonic acidemia

micrognathia

misdiagnosis

mitral valve prolapse

MRI, spinal cord, increased intramedullary cord signal

multiple endocrine neoplasia

muscle atrophy, progressive

muscle atrophy, static

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

myelomalacia

myeloneuropathy

myelopathy

myeloproliferative disorder

myopathy

myopathy, myofibrillar

nerve conduction studies

nerve hypertrophy

neuritis, heavy metals causing

neuroendocrinology

neurologic disease, diagnoses of

neuroma

neuromuscular disease, electrodiagnosis of

neuropathy

neuropathy, ataxic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

neuropathy, sensory

neuropathy, sensory, hereditary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

opened mouth

operculum syndrome, bilateral

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paresthesias, lower extremity

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

peroneal muscle atrophy, causes of

polycythemia, primary

polyglucosan body disease

polymicrogyria

polyneuropathy

polyneuropathy, familial

position sensation, abnormal

posterior column disease

primary thrombocythemia

prognosis

progressive neurologic disorder

proprioception, abnormal

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

pyramidal tract dysfunction

scoliosis, neurologic association with

screening

seizure

sensorineural hearing loss

sensory loss

shoulder, pain in

skin, lesions in neurologic disorders

smell

spasticity

spinal cord, lesion of

steppage gait

sudden death

sweating, abnormality of

synkinesis

tandem gait, ataxic

temporalis muscle wasting

term infant

thrombocytopenia

toe walking

treatment of neurologic disorder

tremor

tremor, intention

trinucleotide repeats

tripping

ultrasonography, nerve

uremia

urine test in toxic screen

uveitis

vibratory sensation, abnormal

vision, blurred

visual evoked response

visual fields, constricted

walking, difficulty with

weakness

weakness, fatiguable

weakness, progressive

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Initial and Follow-up Brain MRI Findings and Correlation with the Clinical Course in Wilson's Disease
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Cladribine in Treatment of Chronic Progressive Multiple Sclerosis
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Thrombocytopenia in Association with Adjunctive Felbamate Use
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Clinicopath Conf
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Hirudin in Acute Myocardial Infarction
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Intracerebral Hemorrhage Complicating Urokinase Infusion Into an Occluded Aortocoronary Bypass Graft
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Myotonic Dystrophy
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Sural Neuropathy Due to External Pressure:Report of Three Cases
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Hyperthermia and Heatstroke
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Coagulation Abnormalities and Cerebral Infarction
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Showing articles 600 to 650 of 831 << Previous Next >>