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Differential
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acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
amyloidosis
anesthesia, general
aneurysm
anterior horn cell disease
areflexia
asymptomatic
bulging of biceps
calf hypertrophy
cardiomegaly
cardiomyopathy
CAT scan
children
chromosome 17
clubfoot as related to neurologic disease
complications
congenital myopathy
congestive heart failure
contractures, joint
creatine phosphokinase(CPK)elevated
delay in diagnosis
developmental retardation
diabetes mellitus
diagnostic criteria
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
dilantin
distal muscle atrophy
distal muscle weakness
dysferlinopathy
dyspnea
dystrophin
dystrophin associated proteins
electromyogram
electron microscopy
enzyme, defect
exercise
facial weakness
falling
familial
fine motor function, impaired
foot drop
gait disorder
gait, waddling
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
Gowers maneuver
hearing loss
hemidiaphragm, paralysis of
hepatomegaly
hereditary myopathy with early respiratory failure
histochemistry
hoarseness
hypercalcemia
hypothyroidism
inability to sit up
Isaacs syndrome
Kobberling-Dunnigan syndrome
Kugelberg-Welander syndrome
learning disability
learning disability, in children
life expectancy
lipodystrophy
liver function enzymes
lordosis
misdiagnosis
molecular genetics
monoclonal gammopathy
motor neuron disease
MRI, muscle
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
muscle swelling
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
myoedema
myoglobinuria
myokymia
myopathy
myopathy, amyloid
myopathy, focal
myopathy, hereditary
myopathy, metabolic
myopathy, monomelic
myopathy, quadriceps
myopathy, vacuolar
nerve conduction studies
neurologic disease, diagnoses of
neurologic examination
neuromyotonia
orthopnea
percussion induced muscle contraction
plasma cell dyscrasia
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
radiculopathy
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
sarcoglycan
sciatic neuropathy
scoliosis
speech disorder, childhood
speech, delayed development of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
steppage gait
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
survival motor neuron gene
systemic illness
telangiectases, retinal
titinopathy
toe walking
tongue, enlarged
tongue, weakness
treatment of neurologic disorder
tripping
urine, dark
vital capacity
weakness
weakness, progressive
weakness, proximal
web sites
wheelchair
winging of scapula
Showing articles 0 to 50 of 131 Next >>

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

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

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,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

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

The Phenotype of Limb-Girdle Muscular Dystrophy Type 21
Neurol 60:1246-1251,1230, Poppe,M.,et al, 2003

Phenotypic Variability in Rippling Muscle Disease
Neurol 52:1453-1459, Vorgerd,M.,et al, 1999

Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
Neurol 48:1227-1234, Eymard,B.,et al, 1997

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Kobberling-Dunnigan Syndrome:A Rare Cause of Generalized Muscular Hypertrophy
Muscle & Nerve 19:843-847996., Wildermuth,S.,et al, 1996

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

Facioscapulohumeral Muscular Dystrophy in Early Childhood
Arch Neurol 51:387-394, Brouwer,O.F.,et al, 1994

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Congenital Monomelic Hypertrophy with Progressive Myopathy
Arch Neurol 48:107-110, Shukla,A.,et al, 1991

Hypertrophy of the Calf with S-1 Radiculopathy
Arch Neurol 45:660-664, Ricker,K.,et al, 1988

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

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Muscular Hypertrophy after Chronic Radiculopathy
Arch Neurol 41:397-398, Montagna,P.,et al, 1984

Isaacs'Syndrome with Muscle Hypertrophy Reversed by Phenytoin Therapy
Arch Neurol 40:241-242, Zisfein,J.,et al, 1983

The Female Carrier of Duchenne Muscular Dystrophy
BMJ 284:1423-1424, Dubowitz,V., 1982

Unilateral Calf Enlargement Following S1 Radiculopathy
Muscle & Nerve 5:434-438982., Mielke,U.,et al, 1982

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

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

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

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

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

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

Cases with IgG4-related Ophthalmic Disease with Mass Lesions Surrounding the Optic Nerve
Am J Ophthalmol 25:101324, Hamaoka, S.,t al, 2022

A 63-Year-Old Woman Presenting with Bilateral Leg Pain
Neurol 96:343-348, Budhu, J.,et al, 2021

CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021

Clinicopathologic Conference, Pheochromocytoma
NEJM 384:1145-1155, Case 9-2021, 2021

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

Immunoglobulin G4-Related Orbital Disease with Bilateral Optic Perineuritis and Maxillary Nerves Involvement:A Case Report
Ophthalmol Ther 9:1089-1099, Hung,C-H., 2020

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

Gummatous Neurosyphilis
Neurol 90:e913-e914, Silva, H.S.,et al, 2018

Clinicopathologic Conference, Cushings syndrome due to a well-differentiated, low-grade thymic neuroendocrine tumor with corticotropin
NEJM 378:2322-2332, Case 18-2018, 2018

Elsberg Syndrome
Neurol Neuroimmunol Neuroinflamm 4:e355-e362, Savoldi, F.,et al, 2017

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 2017

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma Consistent with Neurolymphomatosis
NEJM 376:2471-2481, Case 19-2017, 2017

MR Neurography for the Diagnosis of Hypertrophic Neuropathies
Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017

Bilateral Hypertrophy of Masseteric and Temporalis Muscles, our Fifteen Patients and Review of Literature
Eur Rev Med Pharmacol Sci 20:7-11, Graziano, P.,et al, 2016

Disseminated Cysticercosis
NEJM 375:e52, Baden, L.R., 2016

Diagnostic Criteria for IgG4-Related Ophthalmic Disease
Jpn J Ophthalmol 59:1-7, Goto,JH.,et al, 2015

A 27-year-old Man with Hand Numbness
Neurol 82:e80-e84, Vijayan, J.,et al, 2014

A 61-year-old Woman with a Swollen Optic Nerve and Progressive Visual Loss
Neurol 82:e205-e209, Pecen, P.E. & Bharti, M.T., 2014



Showing articles 0 to 50 of 131 Next >>