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Differential
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advances in neurology
allodynia
amyloidosis
anesthesia, general
anterior horn cell disease
areflexia
arm weakness
asymptomatic
autonomic dysfunction
bone scanning
bulging of biceps
burning paresthesia
calf amyotrophy
calf atrophy
calf hypertrophy
cardiomyopathy
children
Clinical Pathologic Conference(C.P.C.)
creatine phosphokinase(CPK)elevated
cyanosis
descending paralysis
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
DYSF gene
dysferlin
dysferlinopathy
dyspnea
edema, pedal
electromyogram
electron microscopy
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
foot drop
gait disorder
gait, waddling
gene
gene mutation
gene therapy
genetic neurologic disorders
genetic testing
Gowers maneuver
guanethidine
hemidiaphragm, paralysis of
hereditary myopathy with early respiratory failure
hoarseness
hypercalcemia
hyperhidrosis
inability to sit up
India
Kugelberg-Welander syndrome
leg atrophy
leg weakness, unilateral
lid closure, weakness of
life expectancy
livedo reticularis
misdiagnosis
molecular genetics
monoclonal gammopathy
monomelic amyotrophy
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle hypertrophy
muscle swelling
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis, limb-girdle
myoglobinuria
myopathy
myopathy, amyloid
myopathy, hereditary
myopathy, quadriceps
nerve conduction studies
neurologic disease, diagnoses of
neurologic examination
orthopnea
osteoporosis
pain
pain, leg
physical therapy
plasma cell dyscrasia
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
reflex sympathetic dystrophy
reflex sympathetic dystrophy, children
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
scoliosis
shoulder-girdle wasting
skin, temperature difference
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
steppage gait
steroid therapy, CNS treatment and complications with
survival motor neuron gene
sympathetic block
thermography
titinopathy
toe walking
tongue, enlarged
trauma
treatment of neurologic disorder
urine, dark
vital capacity
weakness
weakness, progressive
weakness, proximal
web sites
wheelchair
whistle, inability to
winging of scapula
Showing articles 0 to 50 of 2238 Next >>

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

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

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

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

Amyloid Myopathy Presenting with Distal Atrophic Weakness
Muscle Nerve 29:605-609, Smestad, C.,et al, 2004

Benign Calf Amyotrophy
Arch Neurol 60:1415-1420, Felice,K.J.,et al, 2003

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

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Proximal Weakness of the Extremities as Main Feature of Amyloid Myopathy
JNNP 50:1353-1358, Jennekens,F.G.I.&Wokke,J.H.J., 1987

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

Neurovascular Complications of Iatrogenic Fusarium solani Meningitis
NEJM 390:522-529, Strong, N.,et al, 2024

Calf Hypertrophy and Myoedema Unravel a Diagnosis of Severe Hypothyroidism
Neurol 102:e209138, Camargos, S.,et al, 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

Immunosuppressive Therapy Reversing Obstructive Hydrocephalus in CLIPPERS
Neurol 102:e209396, Yang,Y.,et al, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
Neurologist 29:166-169, Eaton,J.E.,et al, 2024

A 55-Year -Old Woman with Painless Hand Weakness and Atrophy
Neurol 103:e209561, Ticku,H. & Katirji,B.,, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

Ictal Whistling Associated with Dominant Parahippocampal Gyrus Cortical Dysplasia
Neurol 103:e209489, Hartnett,P.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Clinicopathologic Conference, Nutritional Optic Neuropathy Due to Multiple Nutritional Deficits, Including Vitamin A, Copper, and Zinc Deficiencies
NEJM 391:641-650, Gaier,E.D.,et al, 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

Itching Frequency and Neuroanatomic Correlated in Frontotemporal Lobar Degeneration
JAMA Neurol 81:977-984, Hadad,R.,et al, 2024

A 61-Year-Old Man With Progressive Right Leg Numbness and Weakness
Neurol 103:e209900, Jones,F.J.S.,et al, 2024

Clinical Features, Diagnosis and Management of Klinefelter Syndrome
www.UptoDaate.com, Matsumoto,A.M. & Anawals,B.D., 2024

Occipital Condyle Syndrome
Neurol 103:e210067, Mirian,A.,et al, 2024

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Clinicopathologic Conference, Psychotic Disorder Due to a General Medical Condition (postictal psychosis)
NEJM 391:2036-2046, Case 37-2024, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

Leptomeningitis with Communicating Hydrocephalus in an Immunocompromised Patient with Disseminated Sporotrichosis
Neurol 103:e209586, Taborda,M.H.,et al, 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

MR Imaging Findings in Anti-Leucine-Rich Glioma Inactivated Protein 1 Encephalitis:A Systematic Review and Meta-Analysis
AJNR 45:977-986, Almeida,F.C.,et al, 2024

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

IgG4-Related Orbital Inflammation
https://EyeWiki.org, Oct, Chelnis,J. & Gervasio,K.A., 2023

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
Neurol 100:e2027-e2035, Pagnotti,R.M.B.,et al, 2023

Drug Resistant Epilepsy in a 61-Year-Old Man with Abnormal MRI Brain Findings and Management with Vagal Nerve Stimulator
Neurol 100:1111-1116, Mankad,J.P. & Lavingia,J.R., 2023

Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023

Primary Diffuse Leptomeningeal Melanocytosis, A Diagnoatic Conundrum
Neurol 101:e576-3580, Selvarajan,J.M.P.,et al, 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

A 67-YEar-Old Man with Multiple Intracranial Lesions
Neurol 101:e845-e851, Ngo,A.,et al, 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

A Young Woman with Rapidly Progressive Weakness and Paresthesia
Neurol 101:676-681, Alwakeel,S.S.,et al, 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023



Showing articles 0 to 50 of 2238 Next >>