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Differential
(Click to cross reference)
acromicria
amniocentesis
Angelman syndrome
anorexia
antitoxin
apraxia of eye movements
aspartate aminotransferase
ataxia
athetosis
autonomic dysfunction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
bilirubin encephalopathy
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
breast feeding
bulbar palsy
bulbar palsy, childhood
CAT scan, abnormal
cerebral cortical atrophy
cerebrospinal fluid
cerebrospinal fluid, cell count, normal
children
chromosome 15
Clinical Pathologic Conference(C.P.C.)
contractures, joint
cry, abnormal
cry, high-pitched
cry, weak
crying
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
drooling
dysarthria
dysmorphic
dysphagia
eating disorder
efficacy
electroencephalogram, abnormalities of
encephalitis, viral
encephalopathy
enzyme, defect
facial appearance, abnormal
failure to thrive
feeding disorder
fetal movements, reduced
fetus
fever
floppy infant
food poisoning
food-borne infection
gait disorder
gammaglobulin therapy, intravenous
gastroenteritis
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucocerebrosidase
growth hormone deficiency
hand flapping
head bobbing
head lag
hearing loss
hepatic failure
hepatic failure, acute
hepatitis
histochemistry
histochemistry of muscle
honey
hot, red, angry babies
human parechovirus
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hyperphagia
hyperreflexia
hypertension
hypogonadism
hypopigmentation of skin
hyporeflexia
hypotonia
hypotonia, infants
imbalance
infant, evaluation of
infection
intellectual deficit
irritability
irritable baby
jaundice
kernicterus
lactic dehydrogenase(LDH)
Leigh's disease
lethargy
liver function enzymes
meningoencephalitis
mental retardation
merosin
microcephaly
misdiagnosis
mitochondrial disease
molecular genetics
molybdenum cofactor deficiency
moro reflex
mortality
MRI
MRI, abnormal
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
muscle biopsy
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
myoclonic jerks
neck weakness
neurologic disease, diagnoses of
neuromuscular junction, abnormality of
neurotoxin
nystagmus
obesity
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, neonatal
opisthotonus
parechovirus encephalitis
pediatric neurology
polymerase chain reaction
Prader-Labhart-Willi syndrome
premature infant
prenatal diagnosis by amniocentesis
prognosis
psychomotor retardation
ptosis
ptosis, bilateral
rash
rash, hand
respiratory failure
respiratory tract infection
review article
season
seizure
seizure, neonatal
sensorineural hearing loss
septicemia
setting sun phenomena
short stature
spongy degeneration of brain
strabismus
suck, poor
tachycardia
temper tantrums
term infant
tongue, protrusion of
tonic spasms
treatment of neurologic disorder
tremulousness
upgaze, paralysis of
uric acid, low
vertical gaze
viral infection
viral infection, CNS
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, infant
white matter disease
wide based gait
Showing articles 0 to 50 of 146 Next >>

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Inherited Metabolic Diseases of the Nervous System, Infantile Gaucher Disease
Adams & Victors Principles of Neurology, Chp 37, pg 958, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014

Human Botulism Immune Globulin for the Treatment of Infant Botulism
NEJM 354:462-471, Arnon,S.S.,et al, 2006

Mutations in the Molybdenum Cofactor Biosynthetic Genes MOCS1, MOCS2, and GEPH
Hum Mutat 21:569-576, Reiss,J. &Johnson,J.L., 2003

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

Bilirubin Metabolism and Kernicterus
Adv Pediatr 44:173-229, Gourley,G.R., 1997

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Clinicopathologic Conference, Functional Seiaures
NEJM 388:1210-1218, Case 10-2023, 2023

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

Clinicopathologic Conference, Acute human immunodeficiency virus type 1
NEJM 385:641-648, Case 24-2021, 2021

Area Postrema Syndrome as the Initial Presentation of Alexander Disease
Neurol 97:548-549, Renaldo, F.,et al, 2021

Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
NEJM 385:1317-1325, Case 30-2021, 2021

Clinicopathologic Conference, Lead Poisoning
NEJM 385:2378-2388, Case 38-2021, 2021

Cyclic Vomiting Syndrome in Children
AJGH 2:doi:10.33552/AJGH.2020, Al-Ansari, N., 2020

Pernicious Anaemia
BMJ 369:m1319, Mohamed, M.,et al, 2020

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

Carbon Monoxide Poisoning
BMJ 365:DOI.10.136/BMJ.L2299, Ashcroft, J.,et al, 2019

Ehlers-Danlos Syndromes
BMJ 366:I4966, Ghali, N.,et al, 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

A Patient with Psychiatric Illness and Multiple Hemorrhages
JAMA 322:2437-2438, Van Baalen, E.,et al, 2019

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

Neurological Manifestations Among US Government Personnel Reporting Directional Audible and Sensory Phenomena in Havana, Cuba
JAMA 319:1125-1133, 1098, 1079, Swanson, R.L.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Clinicopathologic Conference, Poststroke Mania and the Frontal Lobe Syndrome
NEJM 379:182-189, Case 21-2018, 2018

Spinal Tuberculosis Masquerading Lung Malignancy
Neurol 91:632-633, Garg, R.K.,et al, 2018

Clinicopathologic Conference, Pulmonary Adenocarcinoma, Complicated by a Hypercoagulable State with a Nonbacterial Thrombotic Endocarditis
NEJM, Case 33-2018, 2018

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Clinicopathologic Conference, Advanced AIDS Complicated by HSV-1 Encephalopathy. Basal-Cell Carcinoma. Kaposis Sarcoma.
NEJM 376:2580-2589, Case 20-2017, 2017

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

Clinical Manifestations and Evaluation of Adults with Suspected Native Valve Endocarditis
UpToDate Feb, Sexton, D.J. & Fowler,Jr., V.G., 2016

Neonatal Abstinence Syndrome
NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

Hepatitis Associated with Mycoplasma Pneumoniae Infection in Korean Children:A Prospective Study
Korean J Pediatr 58:211-217, Kim,K.W.,et al, 2015

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

The Acquired Metabolic Disorders of the Nervous System, High-Altitude (mountain) sickness
Adams & Victors Principles of Neurology Chp 40, pg 1139, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Hepatic Stupor and Coma (Hepatic, or Portal-Systemic Encephalopathy)
Adams & Victors Principles of Neurology Chp 40, pg 1142, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Botulism
Adams & Victors Principles of Neurology Chp 43, pg 1218, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Lead
Adams & Victors Principles of Neurology Chp 43, pg 1220, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Inherited Hypeammonemia
Adams & Victors Principles of Neurology, Chp 37, pg 952, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Maple Syrup Urine Disease
Adams & Victors Principles of Neurology, Chp 37, pg 953, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 982, Ropper, A.H.,et al, 2014

A 47-year-old Woman with Left Shoulder Pain after a Fall
Neurol 83:e112-e116, Jerath, N.U.,et al, 2014

Anorexia and Emaciation in Patients with Cerebellar Hemangioblastoma
Neurol 83:1298-1300, Oya, S.,et al, 2014

Polymyalgia Rheumatica
Lancet 381:63-72, Kermani, T. & Washington, K., 2013

Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
NEJM 368:2015-2024, Case 16-2013, 2013



Showing articles 0 to 50 of 146 Next >>