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Differential
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acromegaly
acromicria
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adverse drug reaction
alopecia
amenorrhea
amniocentesis
anemia
aneurysm, intracranial
Angelman syndrome
angiography, cerebral
ankle edema
anosmia
areflexia
arrhythmia, cardiac
arthritis
ascites
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxic gait
autoimmune disease
azospermia
B 12 deficiency
basal ganglia, calcification of
behavior, combative
behavioral disorder
bone marrow transplantation
bromocriptine
cabergoline
cachexia
cafe au lait spots
calcification, intracranial
carcinoma
cardiomyopathy
caries
carotid artery occlusion, intracranial
CAT scan, emission, abnormal
cataracts
celiac disease, adult
celiac disease, childhood
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebrospinal fluid, elevated protein of
cerebrovascular accident
chiasmal syndromes
children
chromophobe adenoma
chromosomal abnormality
chromosome 15
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
coenzyme Q10
coenzyme Q10 deficiency
collateral circulation
complications
contractures, joint
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
cryptorchidism
cultured skin fibroblasts
Cushing's syndrome
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
dermatitis herpetiformis
developmental retardation
diabetes insipidus
diarrhea
diet
dopamine agonist
drooling
dysarthria
dysmetria
dysmorphic
dysphagia
ear, abnormal
eating disorder
efficacy
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
epidemiology of neurology
erectile dysfunction
evoked potentials
exome sequencing
eye movement, disorders of
eyes, sunken
facial appearance, abnormal
failure to thrive
familial
fatty acid, elevated plasma content
feeding disorder
fingers, abnormal
fluorescein angiography
foot drop
F-wave response
gadolinium
gait disorder
galactorrhea
gastrointestinal disease, neurologic complications
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
genital hypoplasia
gluten ataxia
gluten sensitivity
gluten-free diet
gonadotropin-releasing hormone
gray hair
growth hormone
growth hormone deficiency
growth retardation
gynecomastia
hair, loss
hand flapping
headache
hearing loss
hepatitis
hepatosplenomegaly
high arched palate
hirsutism
HLA
hormone replacement
hormone therapy
hyperphagia
hypertelorism
hypodontia
hypogonadism
hypogonadism, hypogonadotropic
hypomyelination
hypopigmentation of skin
hypopituitarism
hyposmia
hypothalamus
hypothalamus, damage to
hypothalamus, disturbance of
hypothyroidism
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
immunodeficiency
immunosuppression
impotence
incoordination
infertility
intellectual deficit
iris, abnormal
Kallmann's syndrome
Klinefelter's syndrome
learning disability
leukodystrophy
leukodystrophy, 4H
leukoencephalopathy
libido
libido, decreased
liver disease
long bone lesion
Lorenzo's oil
magnetic stimulation, brain
malabsorption
menses, irregular
mental retardation
micrognathia
misdiagnosis
molecular genetics
monoclonal gammopathy
mortality
moyamoya
moyamoya, adult
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, spinal cord
muscle biopsy
muscular dystrophy
myeloma, osteosclerotic
myelopathy
myopia
myotonia
myotonia dystrophica
neck weakness
neoplasm, pituitary
neoplasm, pituitary, incidental
neoplasm, pituitary, treatment of
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuronal migration disorder
neuropathy
neuropathy, demyelinating
neuropathy, peripheral
next-generation sequencing
nystagmus
obesity
octreotide
ocular myopathy
oculopharyngeal muscular dystrophy
olfactory bulb
oligomenorrhea
oligospermia
ophthalmoplegia
optic atrophy
optic neuropathy
oral ulcerations
organomegaly
osteoporosis
ovarian dysgenesis
P300
pain, leg
papilledema
paraparesis, spastic
penis, small
perimetry
peroxisomal disease
Perrault syndrome
photosensitivity, skin
pigmentary retinopathy
pituitary
pituitary stalk
pituitary stalk, lesion of
pituitary, adenoma
pituitary, dysfunction
pituitary, hormones of
pituitary, lesion of
pituitary, microadenoma
plasmacytoma
plethora
POEMS syndrome
practice guidelines
Prader-Labhart-Willi syndrome
precocious puberty
prenatal diagnosis by amniocentesis
progeria
progressive neurologic disorder
prolactin
prolactin, elevated
prolactinoma
psychomotor retardation
ptosis
ptosis, familial
puberty
puberty, delayed
pulmonary infiltrates
radiation therapy, CNS treatment and complications with
rash
retinopathy
review article
sarcoidosis
sarcoidosis, CNS
sclerosis, bone
seizure
sella turcica, enlargement of
sensorineural hearing loss
serologic testing
short stature
sinuses, diseases of
skin, darkening of
skin, lesions in neurologic disorders
skull x-ray, abnormal
smell
somatosensory evoked potentials
somatostatin analogue
splenomegaly
steroid therapy, CNS treatment and complications with
stooped posture
strabismus
suck, poor
suprasellar lesion
synkinesis
systemic illness
teeth, abnormal
temper tantrums
temporalis muscle wasting
testicular atrophy
testosterone
testosterone, serum
testosterone, serum, low
third ventricle, wall
thrombocytosis
tongue, protrusion of
treatment of neurologic disorder
tremor
tremulousness
ubiquitination
urinary gonadotropin
vascular endothelial growth factor
visual acuity, decreased
visual field defect
visual fields
visual loss
vitiligo
weakness, generalized
Werner's syndrome
white matter disease
wide based gait
workup
X-linked bulbospinal neuronopathy
Showing articles 0 to 50 of 5924 Next >>

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

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

A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016

Extraintestinal Manifestations of Coeliac Disease
Nat Rev Gastroenterol Hepatol 12:561-571, Leffler, D.A.,et al, 2015

Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
NEJM 368:1992-2003, Margolin, D.,et al, 2013

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Prolactinomas
NEJM 362:1219-1226, Klibanski,A., 2010

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

Sarcoidosis: Clinical, Hormonal, and Magnetic Resonance Imaging (MRI) Manifestations of Hypothalamic-Pituitary Disease in 9 Patients and Review of the Literature
Medicine 86:259-268, Bihan,H.,et al, 2007

Late-Onset Cerebellar Ataxia with Hypogonadism and Muscle Coenzyme Q10 Deficiency
Neurol 62:818-820, Gironi,M.,et al, 2004

Prolactinoma
NEJM 349:2035-2041, Schlechte,J.A., 2003

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Diagnosis and Management of Pituitary Tumours
BMJ 308:1087-1091, Levy,A.&Lightman,S.L., 1994

Hypothalamic-Pituitary Dysfunction after Radiation for Brain Tumors
NEJM 328:87-94, Constine,L.S.,et al, 1993

Cortically Evoked Motor Responses in Patients with Xp22. 3-Linked Kallmann's Syndrome and in Female Gene Carriers
Ann Neurol 31:299-304, Danek,A.,et al, 1992

Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
NEJM 326:1752-1755, 17751992., Bick,D.,et al, 1992

Accelerated Aging of the Brain in Werner's Syndrome
Neurol 42:922-924, Kakigi,R.,et al, 1992

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

Neurologic Findings in Men with Isolated Hypogonadotropic Hypogonadism
Neurol 39:223-226, Schwankhau,J.D.,et al, 1989

Syndrome of Cerebellar Ataxia and Hypogonadotrophic Hypogonadism:Evidence for Pituitary Gonadotrophin Deficiency
JNNP 52:407-409, Fox,A.C.K.,et al, 1989

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Isolated CNS Sarcoidosis
JAMA 245:62-63, Cariski,A.T., 1981

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

Prolactin-Secreting Tumors & Hypogonadism in 22 Men
NEJM 299:847-852, Carter,J.N.,et al, 1978

Adrenomyeloneuropathy:A Probable Variant of Adrenoleukodystrophy
Neurol 27:1107-1113, Griffin,J.W.,et al, 1977

Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence
(Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

Endovascular Therapy for Acute Vertebrobasilar Occlusion (VERITAS): A Systematic Review and Individual Patient Data Meta-Analysis
Lancet 405:61-69, Nogueira,R.G.,et al, 2025

Rocky Mountain Spotted Fever Encephalitis and "Starry Sky" Pattern on MRI, A Case Report
Neurologist 30:34-38, Mikhaiel,J.P.,et al, 2025

Addressing Systemic Complications of Acute Stroke: A Scientific Statement From the American Heart Association
Stroke 56:e15-e29, Kumar,S.,et al, 2025

Cerebrovascular Events in Patients Undergoing Transcatheter Aortic Valve Replacement:A Review
Stroke 55:2754-2764, Patel,K.P.,et al, 2024

Optimal Timing of Anticoagulation after Acute Ischaemic Stroke with Atrial Fibrillation (OPTIMAS): A Multicentre, Blinded-Endpoint, Phase 4, Randomised Controlled Trial
Lancet 404:1731-1741, Werring,D.J.,et al, 2024

Diagnosis of Incident Cancer After Cryptogenic Stroke
Neurol 103:e210027, Navi,B.B.,et al, 2024

2024 Guide for the Primary Prevention of Stroke:A Guideline From the American Heart Association/American Stroke Association
Stroke 55:e344-e424, Bushnell,C.,et al, 2024

Clinicopathologic Conference, Infective Endocarditis Due to Haemophilus Parainfluenza
NEJM 391:2148-2157, Case 38-2024, 2024

Clinical Reasoning: A 39-Year-Old Returning traveler with Acute Encephalopathy and Strokes
Neurol 104:e210177, Buback,ClT.,et al, 2024

Clinicopathologic Conference, Cryptococcal Meningoencephalitis
NEJM 391:2361-2369, Case 40-2024, 2024

Effect of IV Thrombolysis With Alteplase in Patients with Vessel Occlusion in the WAKE-UP Trial
Neurol 104:e209871, Galinovic,I.,et al, 2024

Association of Assisted Reproductive Technology and Stroke During Hospitalization for Delivery in the United States
Stroke 55:999-1005, Dicpinigaitis,A.J.,et al, 2024

Hemorrhagic Strokes Attributable to Chronic Alcohol Consumption and Heavy Episodic Drinking in France
Neurol 102:e209228, Dufour,L.,et al, 2024

Clinical Evaluation of a 2-Minute Ultrafast Brain MR Protocol for Evaluation of Acute Pathology in the Emergency and Inpatient Settings
AJNR 45:379-385, Lang,M.,et al, 2024

Patent Foramen Ovale Management for Secondary Stroke Prevention:State-of-the-Art Appraisal of Current Evidence
Stroke 55:236-247, Sposato,L.A.,et al, 2024

Risk of Stroke and Myocardial Infarction Among Initiators of Triptans
JAMA Neurol 81:248-254, Petersen,C.L.,et al, 2024

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

Diagnosis and Management of ANCA-Associated Vasculitis
Lancet 403:683-698, Kronbichler, A., et al, 2024



Showing articles 0 to 50 of 5924 Next >>