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Differential
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acid maltase deficiency
adverse drug reaction
anasarca
cardiomyopathy
Clinical Pathologic Conference(C.P.C.)
consanguinity
contractures, joint
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
delay in diagnosis
difficulty climbing stairs
drug induced neurologic disorders
dyspnea
electromyogram
enzyme treatment
eosinophilia
eosinophilic fasciitis
exercise intolerance
falling
familial
fibrillations
gemfibrozil
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
groove sign
hammertoes
high arched feet
hip flexor weakness
hip pain
human diploid cell rabies vaccine
hyporeflexia
hypoxia
iatrogenic neurologic disorders
imbalance
leg swelling
leg weakness, bilateral
low back pain
MRI, muscle
muscle biopsy
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
myopathy
myopathy, genetic
myopathy, hereditary
myopathy, metabolic
myopathy, myofibrillar
myopathy, necrotizing
myopathy, toxic
myopathy, vacuolar
myositis
myotonic discharges
neurocutaneous disease
neurologic disease, diagnoses of
pain, back
pain, leg
paraspinal muscle
paresthesias
Pompe's disease of glycogen storage
positive sharp waves
prayer sign
progressive neurologic disorder
proximal muscle atrophy
pulmonary hypertension
renal failure
respiratory failure
rhabdomyolysis
screening
sedimentation rate, elevated
shoulder, pain in
simvastatin
skin, biopsy
skin, lesions in neurologic disorders
skin, thickened
standing difficulty
statin therapy
stiff joints
treatment of neurologic disorder
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
winging of scapula
X-linked myopathy
x-linked myopathy with excessive autophagy
Showing articles 0 to 50 of 177 Next >>

Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023

A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,et al, 2022

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
Neurol 86:e190-e194, McIntosh, P. & Karam, C., 2016

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
NEJM 36:944-954, Case 7-2012, 2012

Severe Myotonic Crisis Resembling Malignant Hyperthermia
Neurol 104:e213497, Wadhwani,A.R.,et al, 2025

Cancer Risk in Patients with Muscular Dystrophy and Myotonic Dystrophy
Neurol 103:e209883, Maya-Gonzalez,C.,et al, 2024

Clinicopathologic Conference, Paraneoplastic Encephalomyelitis Due to Small-Cell Lung Carcinoma and Concurrent Cerebral Amyloid Angiopathy
NEJM< 391357-369, Case 23-2024, 2024

Clinicopathologic Conference, Noncirrhotic hyperammonemia after Roux-en-Y Gastric Bypass
NEJM 389:1221-1230, Case 30-2023, 2023

A 56-Year-Old Man with Unusual Presentation of Subacute Encephalopathy and Seizure
Neurol 98:e95-e102, Wang, T.,et al, 2022

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

Subacute Encephalopathy with Seizures in Alcoholics (SESA) - Related Abnormalities on EEG and MRI
Neurol 99:354-355, Suh, J.,et al, 2022

Clinicopathologic Conference, Fat Embolism Syndrome
NEJM 385:2464-2474, Case 39-2021, 2021

Long Survival Sporadic Creutzfeldt-Jakob Disease
Neurol 95:87-88, Liu, X.Y.,et al, 2020

A Patient with a History of Weight Loss Presenting with Seizures
Neurol 95:e2038-e2042, Tang, G. & Benavides, D.R., 2020

Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
Acta Myologica 37:267-271, Papa, A.A.,et al, 2018

Persistent Respiratory Failure Following Cardiac Arrest
Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 2018

Brain Imaging in Myotonic Dystrophy Type 1
Neurol 89:960-969, Okkersen, K.,et al, 2017

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

An 87-year-old Man with Chronic Obstructive Pulmonary Disease and Acute Encephalopathy
Neurol 87:e135-e139, Spera, K.,et al, 2016

Rapidly Progressive Quadriplegia and Encephalopathy
JAMA Neurol 73:1363-1366, Wynn, D.,et al, 2016

A 64-year-old Man with Visual Distortions
Neurol 87:e252-e256, McGrath, E.R.,et al, 2016

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Herpes Simplex Encephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 751, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Subacute Sclerosing Panencephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 766, Ropper, A.H.,et al, 2014

Infantile Herpes Simplex Encephalitis
Neurol 83:e85-e86, Cappellari, A.M.,et al, 2014

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Electrophysiological Study with Prophylactic Pacing and Survival in Adults with Myotonic Dystrophy and Conduction System Disease
JAMA 307:1292-1301, Wahbi,K.,et al, 2012

Generalised Periodic Discharges in the Critically Ill
Neurol 79:1951-1960,1940, Foreman, B.,et al, 2012

Cancer Risk Among Patients with Myotonic Muscular Dystrophy
JAMA 306:2480-2486, Gadalla, S.M.,et al, 2011

Subacute sclerosing panencephalitis: An Update
Dev Med Child Neurol 52:901-907, Guitierrez, J.,et al, 2010

Mexiletine Is an Effective Antimyotonia Treatment in Myotonic Dystrophy Type 1
Neurol 74:1441-1448, Logigian,E.L., et al, 2010

Prognostic Implications of Periodic Epileptiform Discharges
Arch Neurol 66:985-991, Orta,D.S.,et al, 2009

The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1
NEJM 358:2688-2697, Groh,W.J.,et al, 2008

PLEDS: Clinical Correlates
Can J Neurol Sci 34:443-450, Fitzpatrick,W. &Lowry,N., 2007

Electrographic Seizures and Periodic Discharges After Intracerebral Hemorrhage
Neurol 69:1356-1365, Claasen,J.,et al, 2007

Herpes Encephalitis
eMedicine (Feb), Patel,M.R., 2007

Clinicopath Conf., MELAS Syndrome
NEJM 353:2271-2280, Case 36-2005, 2005

Diffusion-Weighted MRI Abnormalities as an Early Diagnostic Marker for Creutzfeldt-Jakob Disease
Neurol 63:443-449,410, Shiga,Y.,et al, 2004

Severe Cardiac Arrhythmias in Young Patients with Myotonic Dystrophy Type 1
Neurol 63:1939-1941, Bassez,G.,et al, 2004

Sudden Cardiac Death in Myotonic Dystrophy Type 2
Neurol 63:2402-2404, Schoser,B.G.H.,et al, 2004

Myotonic Dystrophy Type 2
Neurol 60:657-664, Day,J.W.,et al, 2003

Generalized Convulsive Status Epilepticus in Creutzfeldt-Jakob Disease
Seizure 12:403-406, Neufeld,M.Y.,et al, 2003

Modafinil Reduces Excessive Somnolence and Enhances Mood in Patients With Myotonic Dystrophy
Neurol 59:1876-1880, MacDonald,J.E.,et al, 2002

Subacute Sclerosing Panencephalitis Clinical and Magnetic Resonance Imaging Evaluation of 36 Patients
J Child Neurol 17:25-29, Ozturk, A.,et al, 2002

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,et al, 2002

Serial EEG During Human Status Epilepticus
Neurol 57:1175-1183, Garzon,E.,et al, 2001

New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
Neurol 54:1218-1221, The International Myotonic Dystrophy Consortium (I, 2000



Showing articles 0 to 50 of 177 Next >>