Neudle.com: "head circumference"

Differential
(Click to cross reference)

abortion, spontaneous

abstinence syndrome

achondroplasia

aciduria

acoustic nerve

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acrocyanosis

acromegaly

acromicria

acute disseminated encephalomyelitis

acute necrotizing encephalitis

addiction, heroin

advances in neurology

adverse drug reaction

agenesis of aqueduct of Sylvius

agenesis of corpus callosum

aggression

Aicardi-Goutieres syndrome

Aicardi's syndrome

alcohol

alcohol, neurologic complications with

Aldrich's syndrome

Alexanders disease

Alexanders disease, adult onset

algorithm

alpha-fetoprotein

altered states of consciousness

anemia

Angelman syndrome

angiotensin-converting enzyme, inhibitors

anosmia

antibiotics, neurologic complications with

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiviral agents

aphasia, conduction

apnea

aqueduct of Sylvius, stenosis

arteriovenous malformation

arteriovenous malformation, cerebral

arthralgia

arthrogryposis multiplex

attention deficit disorder with hyperactivity

autonomic dysfunction

Babinski sign in new born

banana sign

Bannayan-Riley-Ruvalcaba syndrome

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

blood dyscrasias, neurologic findings with

bone density, increased

bone marrow transplantation

Brown-Vialetto-Van Laere syndrome

burst suppression pattern, electroencephalogram

cachexia

cafe au lait spots

calcification, intracranial

calcification, intraventricular

calcification, periventricular

CAT scan, false negative

CAT scan, metrizamide

cataracts

cataracts, congenital

cavum Vergae

Central America

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral gigantism

cerebral palsy

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, protein of

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, intrauterine

cerebrovascular accident, neonatal

cerebrovascular disease, infant and childhood

cherry red spot

chilbran skin lesions

children

chondrodysplasia punctata

chorea

choreoathetosis

chorioretinitis

choroid plexus, tumor of

chromosomal abnormality

chromosome 1

chromosome 15

chromosome 3

cisterna magna, enlarged

cisternogram, radionuclide

cleft lip

cleft palate

Clinical Pathologic Conference(C.P.C.)

clonus

cocaine

cocaine, intrauterine exposure

Cockayne's syndrome

Coffin-Siris syndrome

congenital birth defects

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

consanguinity

constipation

contractures, joint

cornea, opacification in infancy-causes of

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, thinning

cortical blindness

coumarin

cranial neuropathy

cranial neuropathy, multiple

cranial volume

Craniosynostosis

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, high-pitched

cryptorchidism

cultured skin fibroblasts

cyanosis

cyst

cyst, arachnoid

cyst, arachnoid, infant

cyst, arachnoid, location of

cyst, benign intracranial

cyst, parenchymal

cyst, porencephalic

cyst, subcortical

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

cytosine arabinoside

Dandy Walker malformation

deafness

deafness, congenital

deep gray nuclei

degenerative diseases of CNS

dentate nuclei, lesion of

depression

depression, psychotic

dermatitis

dermatoglyphics

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

diencephalic syndrome

diet

differential diagnosis

disability, neurological

dislocated hip, congenital

drooling

drug abuse

drug abuse, toxic screen In

drug withdrawal

dural sinus thrombosis

electroencephalogram, abnormalities of

electroencephalogram, sleep spindles

emergencies, neurologic

encephalitis, brainstem

encephalitis, sequelae in

encephalitis, viral

encephalocele

encephalopathy

encephalopathy, metabolic

enterovirus infection of CNS

epidemiology of neurology

epidermal nevus syndrome

epileptic encephalopathy

episodic disorders

ethics in neurology

ethylmalonic aciduria

ethylmalonic encephalopathy

evoked potentials

exophthalmus

eye movement, disorders of

facial anomalies

facial appearance, abnormal

facial asymmetry

facial expression abnormality

facial nerve palsy

facial nevus

facial weakness

facial weakness, bilateral

fetal alcohol syndrome

fetus

fever

fine motor function, impaired

finger tapping

fingernails, abnormal

fingernails, hypoplastic

fish

flavivirus

floppy infant

fluorescene in situ hybridization

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

geographic location

GFAP gene

glioblastoma multiforme(astrocytoma Gr.III)

GLUT1

GLUT1 deficiency syndrome

growth hormone

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, infantile and childhood form

hand deformity

head bobbing

head circumference

head circumference and brain development

head lag

headache

hearing loss

hearing problems in children

hemangioma

hemifacial spasm

hemihypertrophy, congenital

hemiparesis

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemorrhage, intracranial, newborn

hemorrhagic diathesis

heparin

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, infancy and childhood

herpes simplex encephalitis, prognosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex myelitis

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus infection, newborn

herpes simplex virus, human nervous system and

herpes simplex virus, localization of

herpes simplex virus, malignancy with

herpes simplex virus, pathogenesis of

herpes simplex virus, pathology of

herpes simplex, neurocutaneous lesions in

human immunodeficiency virus type 1

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, etiology

hydrocephalus, exvacuo

hydrocephalus, fetal

hydrocephalus, infants and children

hydrocephalus, intrauterine

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydrocephalus, normal pressure in children

hydrocephalus, treatment of

hydroxyglutaric aciduria

hyperactivity

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperhomocysteinemia

hypernatremia

hyperostosis

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypertrophic cardiomyopathy

hypopigmentation of skin

hypoplastic left heart syndrome

hyporeflexia

hypotelorism

hypothalamus, disturbance of

hypothyroidism

hypothyroidism, congenital

immunofluorescent exam of CSF cells

immunosuppression

in situ hybridization

inborn errors of metabolism

inclusion bodies, intranuclear

increased intracranial venous pressure

infant, evaluation of

infantile spasm

infection

infection, recurrent

infectious mononucleosis

influenza A virus

insect repellent

intellectual deficit

intellectual deterioration

intelligence quotient

interferon

interferon alpha

interferon inducer

interpupillary distance

intracerebral hemorrhage

intracranial hemorrhage

intracranial hypertension, benign

intracranial hypertension, benign, children

intracranial pressure, increased

intrauterine

intrauterine growth retardation

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

klippel feil syndrome

kyphosis

laughing, pathologic

lead poisoning

learning disability, in children

leukoencephalopathy, differential diagnosis

leukotrienes

level of consciousness, decreased

lipid storage disorder of CNS

liver function enzymes

lymphocytic choriomeningitis

lymphoma

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, Vein of Galen

malnutrition and brain development

megalencephaly, idiopathic

menarche

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, chronic

meningitis, CSF cell count-normal

meningitis, neurologic aspects and complications of

mental status, abnormal

mestinon

metabolic disorder, primary

methadone

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

midline defect in children

migraine, seizures in

Miller-Dieker syndrome

misdiagnosis

mitochondrial disease

molecular genetics

molybdenum cofactor deficiency

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, angiography

MRI, CAT scan compared to

mucopolysaccharidoses

mucopolysacchariduria

multiple sclerosis

multiple system atrophy

muscular dystrophy, Duchenne

myoclonus, stimulus sensitive

myopathy

myositis

myotonia dystrophica

myxedema, neurologic manifestations of

neonatal abstinence syndrome

neonatal infection, viral

neoplasm, intracranial

neoplasm, intracranial, congenital

neoplasm, intracranial, infants

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-infants

neoplasm, primary of CNS-survival

nerve root enhancement

neural tube defect

neurocutaneous disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic signs

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neuroradiology

neurosyphilis

nevus

newborn, evaluation of

Noonan Syndrome

nose, abnormal

nutritional deficiency

nystagmus

obesity

old age, neurology of

omphalocele

ophthalmoplegia

opiate

opportunistic infection

optic atrophy

optic atrophy, infants

optic atrophy, unilateral

optic nerve

optic nerve, hypoplasia of

optic nerve, lesion of

optic neuropathy

organoid nevus syndrome

osteogenesis imperfecta

Paget's disease, psychosis in

Paget's disease, spinal cord problem in

pain

palatal myoclonus

palpebral fissure, short

papilledema

paraparesis

paraparesis, familial spastic

paraparesis, spastic

parasitic infection, CNS

parotitis

paroxysmal neurologic deficits

parvovirus

pectus excavatum

pediatric neurology

penis, pigmented macules

periventricular leukomalacia

philtrum, hypoplastic

photosensitivity, skin

pigmentary retinopathy

pigmented macules

pitfalls

pituitary, adenoma

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

polyhydramnios

polyinosinic cytidic acid(poly IC)

polymerase chain reaction

polyps, gastrointestinal tract

pons, atrophy

port wine nevus

posterior fossa, mass of

postural abnormality

practice guidelines

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primitive neuroectodermal tumors

progeria

prognathism

prognosis

progressive neurologic disorder

prolactin, elevated

pruritus

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis

psychosis, childhood

pulmonary stenosis

pupil, abnormality in neurologic disorders

pyramidal tract dysfunction

quadriparesis

quadriplegia

radiation therapy, CNS treatment and complications with

radiation, ionizing

radiation, ionizing, intrauterine

radiculopathy

rash

remote effect of cancer on the nervous system

renal tubular acidosis

respiratory distress syndrome, neurologic status with

respiratory failure

retinal artery occlusion

riboflavin transporter deficiency

scoliosis, neurologic association with

seizure, injury following

seizure, psychomotor-temporal lobe

seizure, withdrawal

sella turcica, enlargement of

sensorineural hearing loss

septo-optic dysplasia

serologic testing

serum alanine aminotransferase

sexual intercourse

sexually transmitted disease

short neck

short stature

shunt procedure, ventricular

shunt procedure, ventricular-complications of

shunt procedure, ventriculo-peritoneal

simian crease

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

skull x-ray, bony defect on

small for dates infant, problems in

speech disorder, childhood

speech, delayed development of

spina bifida

spinal cord, compression of

splenomegaly

spongy degeneration of brain

startle reaction

stem cell transplantation

stereotyped behavior

steroid therapy, CNS treatment and complications with

stillbirth

strabismus

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid fluid collection, benign

subarachnoid hemorrhage

subdural effusion

subdural hematoma

subdural hematoma, neonates and infants

subgaleal fluid collection

subtemporal decompression

suck, poor

sudden infant death syndrome

sulfite oxidase deficiency

superior orbital fissure syndrome

superior sagittal sinus thrombosis

symmetric brain lesions

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

third ventricle, mass of

thrombocytopenia

toe walking

tongue, enlarged

tongue, protrusion of

TORCH infections

toxoplasmosis, CNS

toxoplasmosis, congenital

transilumination of skull

transplacental virus infections

travel, foreign

treatment of neurologic disorder

tremor

trigeminal neuralgia

trinucleotide repeats

trisomes

trisomy 9p

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

uric acid, low

urinary incontinence

urine test for metabolic disorders

vaccinia

valvulopathy

Van der Knaap disease

varicella zoster virus

ventriculogram, metrizamide

ventriculostomy

ventriculostomy, endoscopic

vertebral anomalies

vertebral-basilar insufficiency

viral infection

viral infection, CNS

viral infection, transmission

Virchow-Robin spaces, dilated

visual evoked response

weakness, generalized

weakness, progressive

wheelchair

white matter disease

white matter disease, periventricular

white matter disease, subcortical

Showing articles 0 to 50 of 3117 Next >>

Infantile and Childhood Hydrocephalus
NEJM 387:2067-2073, Whitehead,W.E.&Weiner,J.L., 2022

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

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

An Infant with Developmental Delay, Epileptic Spasms, and Acrocyanosis
Neurol 94:939-942, Madaan, P.,et al, 2020

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Neuroimaging Findings of Zika Virus-Associated Neurologic Complications in Adults
AJNR 39:1967-1974, Hygino da Cruz, L.C.,et al, 2018

Nonmicrocephalic Infarcts with Congenital Zika Syndrome Suspected Only after Neuroimaging Evaluation Compared with Those with Microcephaly at Birth and Postnatally: How Large is the Zika Virus "Iceberg"?
AJNR 38:1427-1434, Aragao, M.F.V.V.,et al, 2017

Zika Virus Associated with Microcephaly
NEJM 374: DOI:10.1056/NEJMoa1600651, Mlakar, J.,et al, 2016

Zika Virus as a Cause of Neurologic Disorders
NEJM 374:1506-1509, Broutet, N.,et al, 2016

Association between Zika Virus and Microcephaly in French Polynesia, 2013-15: a Retrospective Study
Lancet 387:DOI:10.1016/S0140-6736, Cauchemez, S.,et al, 2016

Computed Tomographic Findings in Microcephaly Associated with Zika Virus
NEJM 374:2193-2195, Hazin, A.,et al, 2016

Zika Virus as a Cause of Neurologic Disorders
NEJM 374:1506-1509, Broutet, N.,et al, 2016

Zika Virus
NEJM 374:1552-1563, Petersen, L.R.,et al, 2016

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

Zika Virus as an Emerging Global Pathogen
JAMA Neurol 73:875-879, Beckham, J.D.,et al, 2016

Congenital Zika Virus Syndrome in Brazil: A Case Series of the first 1501 livebirths with complete investigation
Lancet 388:891-897, Franca, G.V.A.,et al, 2016

Zika Virus: An Emergent Neuropathological Agent
Ann Neurol 80:479-489, White, M.K.,et al, 2016

Clinicopathologic Conference, Aqueductal Stenosis with Hydrocephalus
NEJM 375:2583-2593, Case 40-2016, 2016

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

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

Clinicopathologic Conference, Primitive Neuroectodermal Tumor of CNS, with Involvement of Thalamus, Medial Cerebral Cortex, Brainstem, Cerebellum and Subarachnoid Space
NEJM 372:1550-1562, Case 12-2015, 2015

Clinicopathologic Conference, Severe Methylenetetrahydrofolate Reductase Deficiency
NEJM 371:847-858, Case 27-2014, 2014

The Acquired Metabolic Disorders of the Nervous System, Cretinism and Neonatal Myxedema
Adams & Victors Principles of Neurology Chp 40, pg 1156, Ropper, A.H.,et al, 2014

Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients
AJNR 35:402-406, Bhargava, R.,et al, 2014

Cognitive Delay in a 7-year-old Girl
Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013

CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
Neurol 78:1150-1156, Deiva,K.,et al, 2012

Endoscopic Treatment of Hydrocephalus
Arch Neurol 69:664, Walcott, B.P.,et al, 2012

Megaloencephalic Leukoencephalopathy With Subcortical Cysts (Van der Knaap Disease)
Neurol 76:e34, Singh,P.,et al, 2011

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
Neurol 73:887-897, Ashwal,S.,et al, 2009

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
Ann Neurol 62:347-355, Bonthius,D.J.,et al, 2007

Major Congential Malformations After First-Trimester Exposure to ACE Inhibitors
NEJM 354:2443-2451,2498, Cooper,W.O.,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

Vein of Galen Aneurysmal Malformation: Diagnosis and Treatment of 13 Children With Extended Clinical Follow-Up
AJNR 23:1717-1724, Jones,B.V.,et al, 2002

MR Brain Imaging of Fucosidosis Type I
AJNR 22:777-780, Galluzzi,P.,et al, 2001

Pyridostigmine-Induced Microcephaly
Neurol 54:1873-1874, Niesen,C.E.&Shah,N.S., 2000

Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998

Leukotriene C4-synthesis Deficiency:A New Inborn Error of Metabolism Linked to a Fatal Developmental Syndrome
Lancet 352:1514-1517,1487, Mayatepek,E.&Flock.B., 1998

Pitfalls in the Diagnosis of Ventricular Shunt Dysfunction:Radiology Reports and Ventricular Size
Pediatrics 101:1031-1036, Iskandar,B.J.,et al, 1998

Neurodevelopmental Dysfunction Among Nonreferred Children with Idiopathic Megalencephaly
J Pediatr 131:320-324, Sandler,A.D.,et al, 1997

Myotonic Dystrophy, The Role of Large Triplet Repeat Length in the Develop of Mental Retardation
Arch Neurol 54:251-254, Spranger,M.,et al, 1997

Subarachnoid Fluid Collections:A Cause of Macrocrania in Preterm Infants
J Pediatr 128:234-236, AlSaedi,S.A.,et al, 1996

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

White Matter MR Hyperintensities in Adult Patients with Congenital Rubella
AJNR 17:99-103, Barton Lane,E.,et al, 1996

Showing articles 0 to 50 of 3117 Next >>