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

Showing articles 800 to 831 of 831 << Previous

Neurologic Manifestations of Cogan Syndrome
Neurol 28:278, Bicknell,J.M.,et al, 1978

Primary Reticulum Cell Sarcoma of the Brain in Wiskott-Aldrich Syndrome
Arch Neurol 34:633, Model,L.M., 1977

Neurological Complications of Infantile Osteopetrosis
Ann Neurol 2:378, Lehman,R.A.W.,et al, 1977

Spinal Cord Compression Due to Pseudomonas in a Heroin Addict
Neurol 27:1034, Jabbari,B.,et al, 1977

Eosinophilic Polymyositis
Ann Neurol 1:65, Layzer,R.B.,et al, 1977

Superior Sagittal Sinus Thrombosis
Arch Neurol 34:2, Gettelfinger,D.M.,et al, 1977

Bilateral Scalp Necrosis in Temporal Arteritis
Am J Med 61:541, Soderstrom,C.W.,et al, 1976

Case Records of the MGH
Giant cell Angiitis, intracranial NEJM 295:9441976., , 1976

Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
Medicine 55:467, Knox,D.L.,et al, 1976

Neuropsychiatric Manifest. of SLE:Diagnosis, Clinical Spectrum, & Relationship to Other Features of the Disease
Medicine 55:323, Feinglass,E.J.,et al, 1976

Cardiac Myxoma:A Diagnostic Challenge for the Neurologist
Neurol 26:1060, Yufe,R.,et al, 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

The Toxicity of IV Used Marihuana
JAMA 233:251, Payne,R.J.,et al, 1975

Tarsal Tunnel Syndrome
J Am Podiatry Ass 65:825, Kuritz,H.M.,et al, 1975

The Entrapment Neuropathies of Rheumatoid Arthritis
Orth Clin of North Am 6:837-861, Nakano,K.K., 1975

Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence
(Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975

Case Records of MGH-Polycythemia
Carotid Occlusion & Cerebral Infarcts, NEJM 291:96674., , 1974

Case Records of MGH
NEJM 288:363, 1973 288:912, 1973 Cytomegalic Inclusion Disease., , 1973

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

Lymphomatoid Granulomatosis
Human Pathology 3:457, Liebow,A.,et al, 1972

Burning Feet
BMJ Leading Article 3:193, 1972, July., , 1972

The Natural History of SLE by Prospective Analysis
Medicine 50:85, Estes,D.,et al, 1971

The Tarsal Tunnel Syndrome, Diagnosis & Treatment
JAMA 207:716, Edwards,W.G.,et al, 1969

Nonatherosclerotic Causes of Stroke
Ann Int Med 70:807, Levine,J.,et al, 1969

Rocky Mountain Spotted Fever in the Eastern US
NEJM 280:57, Hazard,G.,et al, 1969

Neurologic Syndromes Associated with Primary Thrombocythemia
J Mount Sinai Hosp NY 36:317, Korenman,G., 1969

Neurologic Syndrome Associated With Primary Thrombocythemia
J Mt Siami Hosp 36:317-323, Korenman,G., 1969

Idiopathic Thrombocytosis
Neurol 18:711-713, Levine,J.,et al, 1968

Tarsal Tunnel Syndrome
Jour of Bone & Joint Surg 49B:87967., Lam,S.J.S., 1967

Ocular Complications of Vincristine Therapy
Arch Ophthalmol 78:709, Albert,D.M.,et al, 1967

Neuro CPC of MGH
Thrombotic Throbocytopenic Purpura Involving Brain, NEJM 271:200-2071964., , 1964

Cerebral Hemorrhage In Leukemia
Arch Neurol 2:439-451, Groch,S.N.,et al, 1960

Showing articles 800 to 831 of 831 << Previous