Neudle.com: "facial nerve palsy familial"

Differential
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abdominal muscle paralysis

abducens nerve paralysis

abiotrophy

acetazolamide

acid maltase deficiency

acid maltase deficiency, adult

acoustic nerve

adverse drug reaction

altered states of consciousness

alveolar hypoventilation

amyloidosis

anesthesia, general

anosmia

anterior horn cell disease

anterior tibial muscle weakness

atrioventricular block

autonomic dysfunction

baldness

blind spot, enlarged

blood dyscrasias, neurologic findings with

bone density

bone density, increased

bradycardia

brainstem, dysfunction

CAT scan, base of skull

cataracts

central core disease

cerebritis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, pressure increased

cerebrospinal fluid, pressure low

cerebrovascular accident

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

children

cholesterol, HDL

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

Coats syndrome

compression neuropathy

congenital heart disease

congenital malformation

congenital myasthenic syndromes

corpus callosum, thinning

cough

cranial nerve enlargement

cranial nerve palsies

cranial nerve palsies, familial

cranial nerve palsies, recurrent

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying, pathologic

deafness

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

dementia

denervation of muscle

descending paralysis

developmental retardation

differential diagnosis

diplopia

dislocated hip, congenital

dissociated sensory loss

distal muscle weakness

dropped head syndrome

drug induced neurologic disorders

Duane syndrome

dural sinus thrombosis

electrocardiogram, abnormal

electromyogram

ELISA

Emery-Dreifuss muscular dystrophy

entrapment neuropathy

enzyme, defect

epidemiology of neurology

erythema migrans

face, numbness of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, familial

facial nerve palsy, recurrent

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

granulomatosis with polyangiitis

granulomatous disease

heart block, complete

hematuria, microscopic

Hirschprung's disease

histochemistry

histochemistry of muscle

hyperostosis corticalis generalisata familiaris

hyperostosis cranialis interna

iatrogenic neurologic disorders

immunohistochemistry

impotence

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

intellectual deficit

intracerebral hemorrhage

intracranial hypertension, benign

intracranial hypertension, benign, differential diagnosis

intracranial hypertension, benign, pathogenesis of

intracranial pressure, increased

intrinsic hand muscles, wasting of

isoniazid

jaw pain

klippel feil syndrome

Korsakoff's psychosis

kyphoscoliosis, neurologic causes of

laughing, pathologic

leg weakness, bilateral

leukemia, neurologic findings assoc.with

leukopenia

lid closure, weakness of

lymphoma involving CNS

lymphomatoid granulomatosis

malignant hyperpyrexia

meningismus

meningitis

meningoencephalopathy

menses

methotrexate

methylhydrazine derivatives

micrognathia

misdiagnosis

mitral valve prolapse

molecular genetics

monoamine oxidase inhibitors

mononeuropathy multiplex

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myopathy, distal Laing

myopathy, mitochondrial

myotonia dystrophica, classification

nasal speech

nausea and vomiting

neck weakness

neoplasm, metastatic to CNS

nerve conduction studies

nerve conduction studies, sensory

neurogenic vs.myopathic atrophy

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic evaluation

neuromuscular junction

neuropathy

neuropathy, amyloid

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, vasculitic, systemic

nystagmus, dissociated

ophthalmoplegia, recurrent

optic nerve sheath fenestration

optic nerve, decompression of

optic nerve, lesion of

optic neuropathy

orchitis

orthostatic hypotension

osteosclerosis, autosomal dominant

paraspinal muscle weakness

paratrigeminal syndrome

paresthesias

Parkinson disease

percussion induced muscle contraction

pericarditis

pleocytosis of cerebrospinal fluid

polymyositis

polyneuropathy

pregnancy, neurologic complications in

primary lateral sclerosis

procarbazine

prognathism

prognosis

progressive neurologic disorder

proteinuria

proximal muscle atrophy

pulmonary infiltrates

pyramidal tract dysfunction

scoliosis, neurologic association with

screening

seizure

sensorineural hearing loss

sensory loss, truncal

serologic testing

short stature

shoulder, numbness

shoulder-girdle wasting

shunt procedure, lumboperitoneal

skin, lesions in neurologic disorders

skull x-ray, abnormal

slit lamp examination

spinal muscular atrophy

spinal muscular atrophy, classification

spirochete infection

splenomegaly

spontaneous muscle activity

stent, venous sinus

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

term infant

tetanus

third nerve palsy

third nerve palsy, pupil sparing in

thrombocytopenia

tick bite

tinnitus

tomaculous neuropathy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

transverse smile

treatment of neurologic disorder

trigeminal nerve

trigeminal nerve, lesion of

trigeminal neuralgia

trigeminal neuropathy

trinucleotide repeats

trochlear nerve

trochlear nerve palsy

urine, dark

vertigo

vinblastine

vincristine neurotoxicity

walking, difficulty with

weakness

weakness, fatiguable

weakness, progressive

weakness, proximal

weight loss

wheelchair

whistle, inability to

Wildervanck's syndrome

winging of scapula

wrist drop

Showing articles 0 to 50 of 6156 Next >>

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Pseudotumor Cerebri
Adams & Victors Principles of Neurology, Chp 30, pg 628, Ropper, A.H.,et al, 2014

Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
AJNR 25:494-497, Aho,T.R.,et al, 2004

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Facial Nerve is Liable to Pressure Palsy
Neurol 51:320-322, Foloni,T.E.,et al, 1998

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

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

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Hyperostosis Cranialis Interna
NEJM 322:450-463, Manni,J.J.,et al, 1990

Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Familial Recurrent Bell's Palsy with Ocular Motor Palsies
Neurol 37:1369-1371, Aldrich,M.S.,et al, 1987

Familial Amyloidosis with Cranial Neuropathy & Corneal Lattice Dystrophy
Neurol 36:432-435, Darras,B.T.,et al, 1986

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Recurrent Cranial Nerve Palsies
Clin Pearls 7:4-5, Aziz,N., 1984

Taste & Smell in Disease (First of Two Parts)
NEJM 308:1275-1279, Schiffman,S.S., 1983

Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
Neurol 33:267-277, Stein,S.A.,et al, 1983

Two Cases of Van Buchem's Disease
JNNP 45:913-918, Dixon,J.M.,et al, 1982

Motor Spastic Paraplegia & Unilateral Infra-nuclear Facial Palsy Complicating Tetanus
BMJ 285:477-478, Jain,M.K.,et al, 1982

Familial Recurrent Peripheral Facial Palsy
Arch Neurol 38:463-464, Auerbach,S.H.,et al, 1981

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Duane Syndrome & Congential Upper-Limb Anomalies:A Familial Occurrence
Arch Neurol 34:174, Okihiro,M.M.,et al, 1977

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

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

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

Orbital Apex Syndrome Associated with Herpes Zoster Ophthalmicus
Neurol 104:e213387, Imamura,D.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Progressive Headache and Diplopia in an 89-Year-Old Man
Neurol 104:e213660, Riand,M.,et al, 2025

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

A 63-Year-Old Man With Progressive Multicranial Neuropathy and Leptomeningeal Enhancement
Neurol 103:e210100, Taga,A.,et al, 2024

Behcets Syndrome
NEJM 390:640-651, Saadoun,D.,et al, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Bilateral Hemifacial Spasm and Left Glossopharyngeal Neuralgia Caused by Bilateral Vertebral Artery Displacement
Neurol 102:e209422, Han,Z.,et al, 2024

Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
NEJM 389:166-175, Case 21-2023, 2023

Idiopathic Orbital Inflammation and Tolosa-Hunt Syndrome with Intracranial Extension
Neurol 101:371-374, Yu,S. & Chen,T., 2023

Progressive Cranial Neuropathy
JAMA Neurol 80:1375-1376, Buchberger,D.S.,et al, 2023

Extrapulmonary Manifestations of Sarcoidosis
Rheum Dis Clin North Am 39:277-297, Rao,D.A. & Dellaripa,P.F., 2023

Cavernous Sinus Thrombosis
StatPearls PMID:28846357, Plewa,M.C.,et al, 2023

A 25-Year-Old Woman With Eye Swelling and HEadache
Neurol 100:879-883, Hehir,A.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

Showing articles 0 to 50 of 6156 Next >>