Neudle.com: limb hypertrophy

Differential
(Click to cross reference)

abdominal distention

abducens nerve paralysis

acid maltase deficiency

acid maltase deficiency, adult

advances in neurology

adverse drug reaction

amyloidosis

anesthesia, general

aneurysm

anterior horn cell disease

anticonvulsants

antineurofascin antibodies

autonomic dysfunction

cardiovascular disease

caribbean

CAT scan, emission, abnormal

cataracts

cauda equina

cauda equina, enhancement

cauda equina, lesion of

cavernous sinus

cavernous sinus, lesion of

central nervous system, infection of

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

Charcot-Marie-Tooth

chewing, impaired

children

chromosomal abnormality

chromosome 17

Clinical Pathologic Conference(C.P.C.)

CLOVES syndrome

confusion

congenital malformation

congenital myopathy

congestive heart failure

contactin associated protein like 1 antibodies

contractures, joint

conus medullaris, lesion of

corticotropin level

corticotropin-releasing factor

cortisol, elevated

cranial nerve enlargement

cranial nerve palsies

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Cushing's syndrome

cyst

cysticercosis

cysticercosis, cerebral

cysticercosis, disseminated

cysticercosis, intraventricular

cysticercosis, miliary

cysticercosis, spinal

cysticercosis, subarachnoid

deafness

Dejerine-Sottas syndrome

denervation of muscle

diabetes mellitus

diamond on quadriceps

diaphragmatic paralysis

differential diagnosis

dilantin

diplopia

distal muscle atrophy

distal muscle weakness

dystonia, post traumatic

dystrophin

echocardiogram

echocardiogram, LVH

electrocardiogram, abnormal

electrocardiogram, LVH

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

entrapment neuropathy

enzyme, defect

eosinophilia

ependymitis

epidermal nevus syndrome

exercise

exophthalmus

facial hair, excessive

facial pain

facial pain, atypical

facial weakness

facial weakness, bilateral

failed back syndrome

failed medical management

fine motor function, impaired

foot deformity

foot drop

fourth ventricle, cyst

gadolinium

gait disorder

gait, waddling

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

Gowers maneuver

Guillain Barre syndrome, differential diagnosis of

helminthic infection of CNS

hemiatrophy, congenital

hemidiaphragm, paralysis of

hemihypertrophy, congenital

hemihypertrophy, facial

hemimegalencephaly

hemiparesis

hepatomegaly

hereditary myopathy with early respiratory failure

herniated disc

herniated disc, lumbar

herniated disc, lumbar, recurrent

herniated disc, lumbar-laminectomy

hydrocephalus, non-communicating(obstructive)

hypopigmentation of skin

intracranial pressure, increased

intrinsic hand muscles, wasting of

Isaacs syndrome

Kobberling-Dunnigan syndrome

kyphoscoliosis, neurologic causes of

left ventricular dilatation

leg atrophy

leg numbness

leg swelling

leg weakness, bilateral

leg weakness, unilateral

lumbosacral plexopathy

lymphoma

lymphoma, primary of CNS

lymphopenia

macrocephaly

malformation, CNS, congenital

malignant hyperpyrexia

meningitis, aseptic

meningitis, cysticercosis

meningitis, eosinophilic

mental retardation

mental status, abnormal

monoclonal gammopathy

mononeuropathy

mononeuropathy chronic inflammatory demyelinating

MRI, contrast enhanced

MRI, contrast enhanced, postoperative

MRI, cranial nerves

MRI, lumbosacral plexus

MRI, muscle

MRI, peripheral nerve

MRI, spinal cord

MRI, spine

MRI, spine, postoperative

multiple myeloma

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle hypertrophy

muscle hypertrophy, congenital

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, dystrophin normal

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

neoplasm, hormone producing, ectopic

neoplasm, peripheral nerve

nephrotic syndrome

nerve biopsy

nerve conduction studies

nerve root enhancement

nerve root hypertrophy

neurocutaneous disease

neurologic disease, diagnoses of

neurologic examination

neuropathy, autoimmune

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

night blindness

night sweats

node of Ranvier

nodopathy, autoimmune

nonresponsive

optic nerve, enlarged

parasitic infection, CNS

percussion induced muscle contraction

peripheral nerve, lesion of

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

post polio syndrome

postoperative lumbar spine

postural abnormality

prenatal diagnosis by amniocentesis

prognosis

progressive neurologic disorder

proptosis

proximal muscle atrophy

rippling muscle disease

sedimentation rate, elevated

seizure

sensorineural hearing loss

sensory loss

serologic testing

shoulder, elevation

skin, lesions in neurologic disorders

spinal accessory nerve

spinal cord, compression of

spinal cord, extramedullary cyst of

spinal cord, neoplasm

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, intermediate form

standing difficulty

stem cell transplantation

steppage gait

steroid

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subcutaneous nodules

sudden death

survival motor neuron gene

treatment of neurologic disorder

tremor

trigeminal nerve

trigeminal nerve, hypertrophy

visual acuity, decreased

visual fields, constricted

vital capacity

weakness

weakness, generalized

weakness, progressive

Showing articles 800 to 850 of 1523 << Previous Next >>

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Acquired Neuromyotonia:Evidence for Autoantibodies Directed Against K+Channels of Peripheral Nerves
Ann Neurol 38:714-722, 7011995., Shillito,P.,et al, 1995

Neuromuscular Effects of Papuan Taipan Snake Venom
Ann Neurol 38:916-920, Connolly,S.,et al, 1995

Lumbosacral Plexopathy Due to Benign Uterine Leiomyoma
Neurol 45:1943-1944, Felice,K.J.&Donaldson,J.O., 1995

Neuroradiologic Aspects of Chester-Erdheim Disease
AJNR 16:735-740, Caparros-Lefebvre,D.,et al, 1995

Clinicopath Conf
Arteritis, Unclassified, with Giant-Cell Reaction & Multiple Infarcts of the Brain & Neuropathy, Cas, 5-199532:452-459,1995., 1995

Anterior Communicating Artery Aneurysm Paraparesis Syndrome:Clinical Manifestations and Pathologic Correlates
Neurol 45:45-50, Greene,K.A.,et al, 1995

Clinicopath Conf
Intravascular Lymphomatosis, Case 31-1995, NEJM 333:992-999995., , 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinicopath Conf
Acute Disseminated Encephalomyelitis, (postviral encephalomyelitis) Case 37-1995, NEJM 333:1485-1493, 199, 1995

Renal Cell Carcinomatous Meningitis:Pathologic and Immunohistochemical Features
Neurol 45:189-191, Crino,P.B.,et al, 1995

Classic Neurogenic Thoracic Outlet Syndrome in a Competitive Swimmer:A True Scalenus Anticus Syndrome
Muscle & Nerve 18:229-233995., Katirji,B.&Hardy,R.W., 1995

Clinicopath Conf
Neurolymphomatosis, Case 8-1995, NEJM 332:730-737995., , 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

C-5 Radiculopathy as a Manifestation of Giant Cell Arteritis
Neurol 45:1222-1224, Rivest,D.,et al, 1995

Clinical and Topographical Range of Callosal Infarction:A Clinical and Radiological Correlation Study
JNNP 59:238-242, Giroud,M.&Duman,R., 1995

Medial Medullary Syndrome:Report of 18 New Patients and a Review of the Literature
Stroke 26:1548-1552, Kim,J.S.,et al, 1995

Prolonged Paralysis After Neuromuscular Blockage
Muscle & Nerve, 18:937-94295., Gooch,J., 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995

Alien Hand Syndrome:Interhemispheric Motor Disconnection Due to a Lesion in the Midbody of the Corpus Callosum
Neurol 45:802-808, Geschwind,D.H.,et al, 1995

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

Myelitis Due to Coxsackievirus B Infection
Neurol 45:1626-1627, Jadoul,C.,et al, 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995

Inclusion Body Myositis Presenting with Isolated Erector Spinae Paresis
Neurol 45:993-994, Hund,E.,et al, 1995

Amyloidosis Causing A Progressive Myopathy
Muscle & Nerve 18:1016-1018995., Nadkarni,N.,et al, 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Lambert-Eaton Myasthenic Syndrome (LEMS) in Association with Lymphoproliferative Disorders
Muscle & Nerve 18:715-719995., Argov,Z.,et al, 1995

Pamidronate Treatment of the Neurologic Sequelae of Pagetic Spinal Stenosis
Arch Int Med 155:1813-1815, Wallace,E.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Pain and Remote Weakness in Limbs Injected with Botulinum Toxin A for Writer's Cramp
Lancet 346:154-156, Sheean,G.L.,et al, 1995

Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
Neurol 45:1224-1225, McMorrow,A.M.,et al, 1995

Sciatic Endometriosis:MR Evaluation
AJNR 16:1399-1401, Cottier,J-P.,et al, 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Pott's Paraplegia Today
Lancet 346:264, Miller,J.D., 1995

Radiating Pain to the Lower Extremities Caused by Lumbar Disk Rupture without Spinal Nerve Root Involvement
AJNR 16:1605-1613, 16141995., Milette,P.C.,et al, 1995

Spinal Dural Arteriovenous Fistula:The Pathology of Venous Hypertensive Myelopathy
Neurol 45:1309-1313, Hurst,R.W.,et al, 1995

Neurologic manifestations of intravascular lymphomatosis
Acta Neurol Scand 91:494-499, Chapin, J.E.,et al, 1995

Polyarteritis Nodosa-Induced Quadriplegia
Ann Int MEd 122:731-732, Smith,D.L.,et al, 1995

Radial Tunnel Syndrome. A Retrospective Review of 30 Decompressions of the Radial Nerve
J Hand Surg 20:454-459, Lawrence,T.,et al, 1995

VIIIth Cranial Nerve Involvement in Sarcoidosis
J Laryngol Otol 109:1089-1093, OReilly,B.J. &Burrows,E.H., 1995

MRI in Intraspinal Tuberculosis
Neuroradiology 36:39-43, Gupta,r.K.,et al, 1994

Showing articles 800 to 850 of 1523 << Previous Next >>