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Differential
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abulia
acanthosis nigricans
acrochordon
acromegaly
Addison's disease
adrenal crisis, acute
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
affect, inappropriate
agitation
Albright disease
alcohol, neurologic complications with
alcoholism
alopecia
amenorrhea
aminoacidurias
anasarca
anemia
anemia, megaloblastic
anorexia
anorexia nervosa
anterior horn cell disease
antibiotics
arachnodactyly
areflexia
arteritides
arteritis, temporal
arthralgia
arthritis
ascites
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxic gait
autoimmune disease
B 12 deficiency
B 12 deficiency, infants
Babinski sign
bacterial infection
bacterial infection, CNS
Bannayan-Riley-Ruvalcaba syndrome
basal ganglia, calcification of
behavioral disorder
bladder dysfunction
blindness
bone age
bone marrow biopsy
bone marrow transplantation
bone pain
bone survey
bone survey, metastatic
brain atrophy
brain biopsy
brain scan, abnormal
breast feeding
bulimia
bulimia nervosa
burning hands
burning paresthesia
cachexia
calcification, intracranial
carbamazepine
carpal tunnel syndrome
Castleman's disease
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
CAT scan, disappearing lesion on
cataracts
cathartic
cecum perforation
celiac disease, adult
celiac disease, childhood
central nervous system, infection of
cephalosporins
cerebellar atrophy, secondary
cerebellar degeneration
cerebellum, disease of
cerebral edema
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, red cells in
cerebrovascular accident
chemotherapy, CNS treatment and complications with
children
chorionic gonadotropin
cirrhosis
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
Cockayne's syndrome
coenzyme Q10
coenzyme Q10 deficiency
cognition
cogwheel rigidty
collagenous sprue
coma
compression fracture
confusion
confusional state, acute
congenital malformation
contractures, joint
cortical blindness
cortisol, low
craniopharyngioma
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
crying, pathologic
cultured skin fibroblasts
cyst
cyst, parenchymal
D-dimer
deafness
decerebrate posture
delay in diagnosis
delirium
dementia
dementia, childhood
demyelinating disease
depression
dermal sinus tract
dermatitis
dermatitis herpetiformis
dermoid
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diarrhea
diastematomyelia
diet
dimple
diplopia
dizziness
dysarthria
dysmorphic
dysphagia
dysphasia
dyspraxia
dysproteinemia
dysraphism, spinal
eating disorder
ecchymoses
ectopic pinealoma
edema, leg
edema, pedal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electrophoretic pattern, serum
emergencies, neurologic
emotional lability
encephalomyopathy
encephalopathy
endocarditis, infectious
enzyme, muscle disease
eosinophilia
eosinophilia-myalgia syndrome
eosinophilic fasciitis
epidemiology of neurology
epidermal nevus syndrome
etonogestrel
exercise
exercise intolerance
eye movement, disorders of
face, numbness of
facial anomalies
facial appearance, abnormal
facial nerve
facial nerve palsy
facial pain
facial pain, atypical
familial
fatigue
fatty acid, elevated plasma content
fever
fibrous dysplasia
fibrous dysplasia of orbit
fingernails, abnormal
fingernails, white
fingers, abnormal
folic acid deficiency
follicle stimulating hormone
gait disorder
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glossitis
glossopharyngeal nerve
glossopharyngeal neuralgia
glucose tolerance test, abnormal
gram positive rod
grimacing
groove sign
growth retardation
gynecomastia
hair, darkening of
hand pain
hand weakness
headache
headache, positional
headache, severe
hearing loss
hemangioma
hemochromatosis
hemochromatosis, primary
hemorrhagic diathesis
hepatic encephalopathy
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), screening for
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes simplex virus
herpes simplex virus, human nervous system and
herpes simplex, neurocutaneous lesions in
hirsutism
homocystinuria
hormone replacement
hormone therapy
hydrocephalus
hyperglycemia
hyperhidrosis
hyperhomocysteinemia
hyperkalemia
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypersomnia
hypertrichosis
hypoalbuminemia
hypocalcemia
hypoglycemia
hypoglycemic coma
hypogonadism
hypokalemia
hypomagnesemia
hyponatremia
hyponatremic encephalopathy
hypopigmentation of skin
hypoproteinemia
hypoprothrombinemia
hypotension, systemic
hypothalamus
hypothalamus, disturbance of
hypothalamus, neoplasm of
hypothermia
hypothermia, causes of
hypothyroidism
hypotonia, infants
immunoelectrophoresis, serum
immunosuppressive agents
implant contraceptives
impotence
inappropriate antidiuretic(A.D.H.)hormone
inclusion bodies
inclusion bodies, intracytopasmic
incontinentia pigmenti
infection
insulin resistance
intellectual deficit
intellectual deterioration
intestinal biopsy
intracranial hypertension, benign
intracranial pressure, increased
irritability
jaundice
jaw pain
lactic acidemia
lactic dehydrogenase(LDH)
leg swelling
lethargy
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, toxic
level of consciousness, decreased
lipoma of CNS
lipoma of skin
lipomatosis
liver disease
liver transplantation
Lorenzo's oil
L-tryptophan
luteinizing hormone
lymph node biopsy
lymphadenopathy
lymphoid hyperplasia
lymphoma involving CNS
macrocephaly
malabsorption
malabsorption syndrome
malformation, CNS, congenital
McCune-Albright syndrome
memory, impairment of
mental retardation
mental status, abnormal
methylmalonic acid, serum
microcephaly
misdiagnosis
mitochondrial disease
molecular genetics
monoclonal gammopathy
mononeuritis multiplex
mood change
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, negative
MRI, serial
MRI, spinal cord
MRI, spine
multiple myeloma
muscle biopsy
muscle cramp
muscle pain
muscle weakness
myeloma, osteosclerotic
myelopathy
myoclonus
myoglobinuria
myopathy
myositis
nausea and vomiting
neoplasm, pituitary
nephrotic syndrome
nerve biopsy
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurofibromatosis 1
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuropathy
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neurotoxic
nicotinic acid
night blindness
nutritional deficiency
nystagmus
oculomasticatory myorhythmia
ophthalmoplegia
optic atrophy
orange peel appearance of skin
organomegaly
osteopetrosis
osteoporosis
pain
pain, abdominal
pain, leg
papilledema
paradichlorobenzene
paraparesis
paraparesis, spastic
paresthesias
paresthesias, hands
PAS positive
PAS positive material in the brain
pellagra
penis, pigmented macules
peripheral blood smear, abnormal
pernicious anemia
peroxisomal disease
perseveration
personality change
petechiae
phlebotomy
photophobia
photosensitivity, skin
pigmentary retinopathy
pigmented macules
pituitary, adenoma
plasma cell dyscrasia
plasmacytoma
pleocytosis of cerebrospinal fluid
pleural effusion
pleurisy
POEMS syndrome
polycythemia, primary
polycythemia, secondary
polymerase chain reaction
polymyalgia rheumatica
polyneuropathy
polyps, gastrointestinal tract
post herpetic neuralgia
posterior column disease
precocious puberty
prenatal diagnosis by amniocentesis
progeria
prognosis
progressive neurologic disorder
prolactin, elevated
pruritus
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis, unilateral
pupil, dilated, unilateral
quadriparesis
quadriplegia
radiation therapy, CNS treatment and complications with
rash
Raynaud's phenomenon
refractory sprue
remote effect of cancer on the nervous system
renal failure
reticulum cell sarcoma
review article
rhabdomyolysis
rigidity
Romberg's sign
scalp necrosis
sclerosis, bone
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
shock, hypovolemic
short stature
skin, biopsy
skin, darkening of
skin, discoloration
skin, lesions in neurologic disorders
skin, thickened
skull x-ray, abnormal
skull x-ray, bony defect on
somnolence
spasticity
spina bifida
spinal cord, lesion of
splenomegaly
sprue
steatorrhea
stem cell transplantation
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
superior sagittal sinus thrombosis
systemic illness
teratoma
testicular atrophy
testicular biopsy
tetany
tethered spinal cord
third ventricle, mass of
thrombocytosis
tongue, black
tongue, discoloration
tongue, smooth
tongue, swelling
treatment of neurologic disorder
tremor
tremor, intention
trigeminal neuropathy
trigeminal neuropathy, sensory
trimethoprim-sulfamethoxazole
urine osmolality, elevated
urine, dark
urticaria
uveitis
vascular endothelial growth factor
vegetarianism
very long chain fatty acids
viral infection
Virchow-Robin spaces, dilated
vision, blurred
visual acuity, decreased
visual evoked response
visual loss
visual loss, slow
vitamin B3, deficiency
vitamin deficiency
vomiting, recurrent
weakness
weakness, generalized
weight gain
weight loss
Whipple's disease
white matter disease
whites
x-ray, lumbar spine
Showing articles 0 to 50 of 1307 Next >>

Hyperpigmentation in Vitamin B12 Deficiency
NEJM 386:172, Sherman, S.V., 2022

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Clinicopathologic Conference, Primary Adrenal Insufficiency (Addisons Disease)
NEJM 376:1159-1167, Case 9-2017, 2017

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

A Young Woman with Blurred Vision and Distal Paresthesias
JAMA Neurol 72:1519-1523, Kung, N.H.,et al, 2015

A 12-Year Old Child with Fever, Headache, Shock and Coma
Lancet 385:576, Amores-Hernandez, I.,et al, 2015

Diseases of the Nervous System Caused by Nutritional Deficiency, Pellagra (Niacin, Nicotinic Acid, B3 Deficiency)
Adams & Victors Principles of Neurology Chp 41, pg 1170, Ropper, A.H.,et al, 2014

Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients
AJNR 35:402-406, Bhargava, R.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
Adams & Victors Principles of Neurology, Chp 32, pg 710, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
NEJM 368:2015-2024, Case 16-2013, 2013

Heterogeneity of Coenzyme Q10 Deficiency
Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Black Tongue Due to Adrenocortical Insufficiency
Arch Dis Child 97:1033, de Benedictis, F.M.,et al, 2012

Addisons Disease
Contemp Clin Dent 3:484-486, Sarkar, S.B.,et al, 2012

Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007

Neurologic Presentation of Whipple Disease
Medicine 81:443-457, Gerard,A.,et al, 2002

Muscle Pain after Exercise
Lancet 353:1062, Nielen,C.&Mazzone,P., 1999

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Skin Lesions of the Spinal Axis and Spinal Dysraphism:Fifteen Cases & Review of the Literature
Arch Pediatr Adolesc Med 148:740-748, McAtee-Smith,J.,et al, 1994

POEMS Syndrome:A Study of 25 Cases and a Review of the Literature
Am J Med 97:543-553, Soubrier,M.J.,et al, 1994

Wilson's Disease:Current Status
Am J Med 92:643-654, Yarze,J.C.,et al, 1992

Clinicopath Conf
PEOMS Syndrome, Case 39-1992, NEJM 327:1014-1021992., , 1992

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Pituitary Adenoma in McCune-Albright Syndrome:MR Demonstration
J Comput Assist Tomogr 13:685-688, O'Laughlin,R.L.,et al, 1989

Brain Malformations in Linear Nevus Sebaceous Syndrome:An MR Study
J Comput Assist Tomogr 12:338-340, Sarwar,M.&Schafer,M.E., 1988

Clinicopath Conf
Castleman's Disease, Synd of Polyneuropathy, Organomegally, Endocrinopathy, Monoclonal Gammopathy, &, Skin CPOEM Synd),NEJM 316:606-618,1987., 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Peripheral Neuropathy Associated with Dysproteinaemia, Skin Changes, & Endocrinopathy
BMJ 292:1415-1416, Burton,J.L., 1986

Osteosclerotic Myeloma & Peripheral Neuropathy
Neurol 33:202-210, Kelly,J.J.,et al, 1983

Plasma Cell Dyscrasia with Polyneuropathy, Organomegaly, Endocrinopathy, M Protein, & Skin Changes:The POEMS Syndrome
Medicine 59:311-322, Bardwick,P.A., 1980

Clinical Pathological Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 18-1979, NEJM 300:1037-104579., , 1979

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
NEJM 299:317, Higginbottom,M.C., 1978

Celiac Sprue & Refractory Sprue
Gastroenter. 75:3071978., Trier,J.S.,et al, 1978

CT Scanning & Diagnosis of Adrenoleukodystrophy
Neurol 27:884, Greenberg,H.S.,et al, 1977

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

Polyneuropathy, Skin Hyperpigmentation, Edema, & Hypertrichosis in Localized Osteosclerotic Myeloma
Neurol 27:675, Iwashita,H.,et al, 1977

Herpes Simplex Neuropathy
Neurol 26:596, 1976, Krohel,G.B.,et al, 1976

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

Germinoma of third Ventricle (Case Record of MGH)
NEJM 293:653, Locke,S.,et al, 1975

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Fibrous Dysplasia, In Neurology In Pediatrics
(Ed) , 1970 Year Book Med. Publishers, p. 165., Bray,P.F., 1970

Whipple's Disease:A Review of 19 Pnts from one Hospital & a Review of the Literature since 1950
Medicine 49:175, Maizel,H.,et al, 1970

Addison's Disease, In The Diagnosis of Stupor & Coma
& Posner, J. , FA Davis Co. 1966, p. 145-146., Plum,F., 1966

Clinical and Imaging Features of Cobb Syndrome
Neurol 102:e208118, Yang,X.,et al, 2024

A 30-Year-Old Woman Presenting with Rapidly Progressive Dementia and Extreme Hypoglycorrhachia
Neurol 102:e209188, Bai,X.,et al, 2024



Showing articles 0 to 50 of 1307 Next >>