Neudle.com: dysautonomia familial

Differential
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abdominal cramps

abducens nerve paralysis

acoustic nerve

adult polyglucosan body disease

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

attention deficit disorder with hyperactivity

autonomic dysfunction

autonomic dysfunction, acute

autonomic nervous system

autonomic neuropathy

autonomic neuropathy, idiopathic

blood dyscrasias, neurologic findings with

botulism

bradycardia

brainstem, infarction of

CAT scan, emission, abnormal

cataracts

cataracts, congenital

catecholamine

cerebellar atrophy, secondary

cerebral cortical atrophy

cerebral ischemia

cerebral vasculature

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, pressure low

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chewing movements

chorea

choreoathetosis

cingulate island sign

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

coat-hanger pain

coma

confabulation

congestive heart failure

constipation

cranial neuropathy, multiple

degenerative diseases of CNS

dementia

dementia, familial

dementia, rapidly progressive

developmental retardation

drug induced neurologic disorders

dysarthria

dysmorphic

dystonia

dystonia musculorum deformens

facial nerve palsy, bilateral

fatal familial insomnia

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

gait disorder

gait, spastic

gamma amino butyric acid

genetic neurologic disorders

genetic testing

Gilles de la Tourette syndrome

glycogen storage disease

hepatic encephalopathy

hepatic encephalopathy, treatment of

homovanillic acid

Horner's syndrome

human immunodeficiency virus type 1

hypotension, neurologic causes of

hypotension, systemic

hypotonia

imbalance

impotence

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inattention

inclusion bodies

inclusion bodies, intranuclear

insight, loss

insomnia

intellectual deficit

intellectual deterioration

intrinsic hand muscles, wasting of

Korsakoff's psychosis

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

lipid storage disorder of CNS

marche a petits pas

masked facies

memory, defect of recent

memory, impairment of

meningismus

meningoencephalopathy

mental retardation

methotrexate

methylhydrazine derivatives

misdiagnosis

monoamine oxidase inhibitors

MRI, CAT scan compared to

MRI, diffusion weighted

multiple endocrine neoplasia

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

myocardial infarction

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neuroma

neuronal intranuclear inclusion disease

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, sensory, hereditary

neuropathy, work up for

neurotoxin

neurotransmitter

next-generation sequencing

orthostatic hypotension

orthostatic hypotension, idiopathic

pain

pain, anal

paraparesis

paratrigeminal syndrome

paresthesias

Parkinson disease

Parkinson disease, atypical

Parkinson disease, familial

Parkinsonism syndrome

paroxysmal extreme pain disorder

paroxysmal neurologic deficits

peroneal muscle atrophy, causes of

phenylketonuria

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polyneuropathy, familial

precipitating factors

prion disease

procarbazine

prognosis

progressive neurologic disorder

pyramidal tract dysfunction

seizure, differential diagnosis of

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

shoulder, pain in

Shy-Drager syndrome

sick sinus syndrome

skin, lesions in neurologic disorders

sleep pathology and physiology

smell

SNCA duplication

sodium channel dysfunction

spasticity

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 3/Machado Joseph disease

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, intention

trichopoliodystrophy

trinucleotide repeats

vincristine neurotoxicity

viral infection

visual loss, transient

vocal cord paralysis

weakness

weakness, progressive

weight loss

white matter disease

wrist drop

Showing articles 850 to 900 of 1916 << Previous Next >>

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

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
Radiology 195:35-40, Ronkainen,A.,et al, 1995

Familial Occurrence of Cluster Headache
JNNP 58:341-343, Russell,M.B.,et al, 1995

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

Contralateral Hyperhidrosis after Cerebral Infarction:Clinicoanatomic Correlations in Five Cases
Stroke 26:896-899, Kim,B.S.,et al, 1995

Outcome in Familial Subarachnoid Hemorrhage
Stroke 26:961-963, Bromberg,J.E.C.,et al, 1995

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
Neurol 45:1086-1091, Chabriat,H.,et al, 1995

Autonomic and Thermal Sensory Symptoms and Dysfunction After Stroke
Stroke 26:1379-1385, Naver,H.,et al, 1995

Asymmetrical Skin Temperature in Ischemic Stroke
Stroke 26:1543-1547, Korpelainen,J.T.,et al, 1995

Diminished Nocturnal Blood Pressure Decline and Lesion Site in Cerebrovascular Disease
Stroke 26:829-833, Yamamoto,Y.,et al, 1995

Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
Stroke 26:885-890, Simioni,P.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

Botulinum Toxin Treatment of Essential Head Tremor
Neurol 45:822-824, Pahwa,R.,et al, 1995

The Effect of Nimodipine on Essential Tremor
Neurol 45:1523-1525, Biary,N.,et al, 1995

Autonomic and Peripheral Neuropathies in Patients with Chronic Alcoholism
Arch Neurol 52:45-51, Monforte,R.,et al, 1995

Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
Neurol 45:492-497, Kattapong,V.J.,et al, 1995

Subarachnoid Hemorrhage and Family History:A Population-Based Case-Control Study
Arch Neurol 52:202-204, Wang,P.S.,et al, 1995

Hereditary Late-Onset Chorea Without Significant Dementia:Genetic Evid for Phenotypic Variation in Huntington's Disease
Neurol 45:443-447, Britton,J.W.,et al, 1995

Tourette's Syndrome:A Model Neuropsychiatric Disorder
JAMA 273:498-501, Hyde,T.M.&Weinberger,D.R., 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Hereditary Leukoencephalopathy and Palmoplantar Keratoderma:A New Disorder with Increased Skin Collagen Content
Neurol 45:331-337, 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

A Positron Emission Tomography Study of Cerebral Activation Associated with Essential and Writing Tremor
Arch Neurol 52:299-305, Wills,A.J.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Anticonvulsant Hypersensitivity Syndrome
Arch Int Med 155:2285-2290, Vittorio,C.C.&Muglia,J.J., 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

Lambert-Eaton Myasthenic Syndrome:Clinical Diagnosis,Immune-Mediated Mechanisms,and Update on Therapies
Ann Neurol 37:S63-S73, Sanders,D.B., 1995

Familial Atrioventricular Septal Defect:Possible Genetic Mechanisms
Br Heart J 71:79-81, Kumar,A.,et al, 1994

Benign Familial Nocturnal Alternating Hemiplegia of Childhood
Neurol 44:1812-1814, Andermann,E.,et al, 1994

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

Epidemic Neuropathy in Cuba:A Plea to End the United States Economic Embargo on a Humanitarian Basis
Neurol 44:1784-1786, Roman,G.C., 1994

Increased Risk of Parkinson's Disease in Parents and Siblings of Patients
Ann Neurol 36:659-661, Payami,H.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Clinicopathologic Correlations of HIV-1-Associated Vacuolar Myelopathy:An Autopsy-Based Case-Control Study
Neurol 44:2159-2164, DalPan,G.J.,et al, 1994

Autonomic Involvement in Guillain-Barre Syndrome:A Review
Muscle & Nerve 17:1145-1155994., Zochodne,D.W., 1994

Superoxide Dismutase and ALS
Lancet 344:1651-1652, Orrell,R.W.&deBelleroche,J.S., 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Lower Cognitive Performance in Normal Older Adult Male Twins Carrying the Apolipoprotein E-E4 Allele
Arch Neurol 51:1189-1192, Reed,T.,et al, 1994

On the Inheritance of Intracranial Aneurysms
Stroke 25:2028-2037, Schievnink,W.I.,et al, 1994

Periventricular Heterotopia and Epilepsy
Neurol 44:51-55, Huttenlocher,P.R.,et al, 1994

Increased Risk of Alzheimer's Disease in Mothers of Adults with Down's Syndrome
Lancet 344:353-356, Schupf,N.,et al, 1994

Familial Alzheimer's Disease
Ann Neurol 36:335-336, Bird,T.D., 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Showing articles 850 to 900 of 1916 << Previous Next >>