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Differential
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abdominal reflex, absent
acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
allodynia
amyloid
amyloidosis
anesthesia, general
aneurysm
ankle edema
anterior horn cell disease
areflexia
arm weakness
ascending paralysis
asymptomatic
autonomic dysfunction
beriberi
bone scanning
bulging of biceps
burning paresthesia
calf amyotrophy
calf atrophy
calf hypertrophy
cardiomegaly
cardiomyopathy
CAT scan
cauda equina, enhancement
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
children
chromosome 17
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
complications
compression neuropathy
congenital myopathy
congestive heart failure
contractures, joint
cough
cranial nerve enhancement
cranial nerve palsies, bilateral
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cyanosis
delay in diagnosis
denervation potentials
descending paralysis
developmental retardation
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diabetic mononeuropathy
diagnostic criteria
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
dilantin
distal muscle atrophy
distal muscle weakness
DYSF gene
dysferlin
dysferlinopathy
dyspnea
dystrophin
dystrophin associated proteins
edema, leg
edema, pedal
edema, periorbital
electromyogram
electron microscopy
enzyme, defect
exercise
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
fatigue
femoral nerve
femoral neuropathy
fever
fibrillations
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
guanethidine
hearing loss
hemidiaphragm, paralysis of
hepatomegaly
hereditary myopathy with early respiratory failure
histochemistry
hoarseness
hypercalcemia
hyperhidrosis
hypoglycorrhachia
hyporeflexia
hypothyroidism
inability to sit up
India
influenza A virus
influenza B virus
Isaacs syndrome
Kobberling-Dunnigan syndrome
Kugelberg-Welander syndrome
lateral cutaneous nerve of calf
learning disability
learning disability, in children
leg atrophy
leg weakness, unilateral
lethargy
lid closure, weakness of
life expectancy
lipodystrophy
livedo reticularis
liver function enzymes
lordosis
lymphoma
lymphoma, primary of CNS
meningeal enhancement
mental status, abnormal
misdiagnosis
molecular genetics
monoclonal gammopathy
monomelic amyotrophy
mononeuropathy
mononeuropathy, idiopathic
mononeuropathy, sensory
motor neuron disease
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, muscle
MRI, spinal cord
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
muscle swelling
muscle tenderness
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, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
myasthenia gravis, limb-girdle
myoedema
myoglobinuria
myokymia
myopathy
myopathy, amyloid
myopathy, focal
myopathy, hereditary
myopathy, metabolic
myopathy, monomelic
myopathy, painful
myopathy, quadriceps
myopathy, vacuolar
myositis
myositis, acute of childhood
myositis, post infectious
nerve conduction studies
neurologic disease, diagnoses of
neurologic examination
neuromyotonia
neuropathy
neuropathy, motor
ophthalmoplegia
orthopnea
osteoporosis
pain
pain, calf
pain, leg
percussion induced muscle contraction
periarteritis nodosa
peroneal nerve
peroneal nerve, lesion of
physical therapy
plasma cell dyscrasia
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
ptosis, bilateral
radiculopathy
rapidly progressing neurologic illness
reflex sympathetic dystrophy
reflex sympathetic dystrophy, children
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
saphenous nerve
sarcoglycan
sciatic neuropathy
scoliosis
sedimentation rate, elevated
shoulder-girdle wasting
skin, temperature difference
speech disorder, childhood
speech, delayed development of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
standing difficulty
steppage gait
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
sural nerve
survival motor neuron gene
sympathetic block
systemic illness
telangiectases, retinal
tenderness
thermography
thiamine deficiency
third nerve palsy
titinopathy
toe walking
tongue, enlarged
tongue, weakness
trauma
treatment of neurologic disorder
tripping
urine, dark
viral infection
viral myopathy
vital capacity
vitamin deficiency
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
web sites
wheelchair
whistle, inability to
wide based gait
winging of scapula
Showing articles 0 to 37 of 37

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

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

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

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

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

Clinical Reasoning: A 12-year-old Boy with Ascending Weakness
Neurol 80:e110-ee114, French, K.F.,et al, 2013

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

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

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

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

Benign Acute Childhood Myositis, Laboratory and Clinical Features
Neurol 53:2127-2131, Mackay,M.T.,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

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

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

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

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

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

Idiopathic, Progressive Mononeuropathy in Young People
Arch Neurol 50:20-23, Engstrom,J.W.,et al, 1993

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

Polyarteritis Manifesting as Calf Myositis & Fever
Am J Med 80:312-315, Ferreiro,J.E.,et al, 1986

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

Bilateral Involvement of the Lateral Cutaneous Nerve of Calf in a Diabetic
Ann Neurol 4:480-481, Finelli,P.F.,et al, 1978

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



Showing articles 0 to 37 of 37