Neudle.com: hypotonia infants

Differential
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abdominal distention

acetylcholine receptor antibody

acid maltase deficiency

aciduria

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acrocyanosis

acromicria

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

airway obstruction

alternating hemiplegia

alternating hemiplegia of childhood

anemia, megaloblastic

Angelman syndrome

angiokeratoma

anorexia

anterior horn cell disease

arthrogryposis multiplex

attention deficit disorder with hyperactivity

atypical

autism

autonomic dysfunction

B 12 deficiency

B 12 deficiency, infants

Babinski sign in new born

bacterial infection

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bone density, increased

bone marrow transplantation

botulinum toxin

botulism

botulism antitoxin

botulism immune globulin

Brown-Vialetto-Van Laere syndrome

bulbar palsy

bulbar palsy, childhood

calcification, intracranial

Canavan's disease

canned food

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

cardiomyopathy

CAT scan

CAT scan, abnormal

celiac disease, childhood

central core disease

central nervous system, infection of

cerebellar atrophy, primary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar vermis

cerebral cortical atrophy

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, neonatal

cerebrovascular accident, postpartum

cervical spine injury

cherry red spot

chilbran skin lesions

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

cognition

cognitive delay

coma

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital myopathy

congenital myopathy, inflammatory

corpus callosum, thinning

cortical blindness

cranial neuropathy

cranial neuropathy, multiple

Craniosynostosis

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyanosis

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

deep gray nuclei

delay in diagnosis

delayed dentition

delivery, complicated

dementia

dementia, childhood

dentate nuclei

dentate nuclei, lesion of

descending paralysis

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diagnostic criteria

diarrhea

diet

differential diagnosis

diphtheria-tetanus-pertussis immunization

dislocated hip, congenital

DNA sequencing

drooling

drug overdose

dural sinus thrombosis

electroencephalogram, abnormalities of

electromyogram

electron microscopy

embolism, paradoxical

encephalitis

encephalomyelitis

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

enzyme, defect

epidemiology of neurology

epileptic encephalopathy

evoked potentials

exome sequencing

eye movement, disorders of

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

fetal movements, reduced

fetus

fever

fibrillations

fine motor function, impaired

fundus, abnormality of

gag reflex, depressed

gait disorder

gait, apraxic

gammaglobulin therapy, intravenous

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital hypoplasia

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1

GLUT1 deficiency syndrome

gluten-free diet

glycogen storage disease

glycoprotein

Gowers maneuver

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, infantile and childhood form

hemorrhage, intracranial, newborn

hemorrhage, periventricular

hemorrhagic diathesis

histochemistry of muscle

Horner's syndrome, bilateral

Horner's syndrome, congenital

human genome

Hunter's syndrome

hydrocephalus

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydroxyglutaric aciduria

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperhomocysteinemia

hyperphagia

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypertrophic cardiomyopathy

hypodontia

hypogammaglobulinemia

hypopigmentation of skin

hypoxic encephalopathy

imbalance

immunization, neurologic complications with

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

infant, evaluation of

infantile neuronal degeneration

infantile spasm

infection, recurrent

intellectual deficit

intellectual deterioration

interferon alpha

intestinal biopsy

intracranial hemorrhage

intracranial pressure, increased

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

kyphoscoliosis, neurologic causes of

lactic acidemia

leg weakness, bilateral

lid closure, weakness of

lissencephaly

listeria monocytogenes

liver disease

liver function enzymes

lumbar puncture

lysosomal storage disease

macrocephaly

malabsorption

malformation, CNS, congenital

malformation, vascular

malignant hyperpyrexia

McArdle's disease

meningitis, carcinomatous

meningitis, CSF cell count-normal

mental retardation

merosin

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylmalonic acidemia

microcephaly

micrognathia

micropthalmia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, seizures in

misdiagnosis

mitochondrial disease

mitral valve prolapse

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, fetal

MRI, high signal foci on

MRI, muscle

MRI, spinal cord

MRI, spine

mucopolysaccharidoses

mucopolysacchariduria

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle diseases, characteristics of

muscle phosphorylase deficiency

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscle-eye-brain disease

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, LAMA2

myasthenia gravis, neonatal

myopathy, centronuclear

nemaline rod myopathy

neonatal infection, viral

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

nerve conduction studies

nerve conduction studies, motor

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathology

neuropathology, brain

neuropathy

neurophysiology

neurotoxin

newborn, evaluation of

obstetric neurologic injuries

opened mouth

ophthalmoplegia

ophthalmoplegia, neonatal

ophthalmoplegia, total

optic atrophy

optic atrophy, infants

optic nerve, hypoplasia of

osteopetrosis

pachygyria

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pathology

patient information and support

pectus excavatum

pediatric neurology

periventricular leukomalacia

pertussis immunization

petechiae

phenylketonuria, variant form of

PICU

placenta

placenta, infection of

placenta, thrombosis of

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

poliomyelitis

poliomyelitis vaccine

POLR3B

polyhydramnios

polymerase chain reaction

polymicrogyria

polymyositis

polymyositis, infantile

pons, atrophy

pons, lesion of

postoperative neurologic complications

postpartum

Prader-Labhart-Willi syndrome

precipitating factors

precocious puberty

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prognosis

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, acute

quadriplegia

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

recurrent

reflex, stretch

reflex, tonic stretch

renal tubular acidosis

repetitive nerve stimulation

respirator

respiratory arrest

respiratory depression

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

Rett's syndrome

review article

RFLPs

riboflavin transporter deficiency

rigid spine syndrome

rubella vaccine

scoliosis

scoliosis, neurologic association with

screaming

screening

segmental demyelination

seizure

seizure, children

seizure, focal

seizure, injury following

seizure, neonatal

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

serum alanine aminotransferase

short stature

shunt procedure, ventricular

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray, abnormal

small for dates infant, problems in

SMN1 gene

spastic diplegia

spasticity

speech disorder, childhood

speech, delayed development of

spinal cord, enlargement

spinal cord, injury of

spinal cord, injury, New Born

spinal cord, intramedullary cyst of

spinal cord, transection

spinal muscular atrophy

spinal muscular atrophy, classification

splenomegaly

spongy degeneration of brain

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

subdural effusion

subdural hematoma, neonates and infants

subgaleal hematoma

suck, poor

superior sagittal sinus thrombosis

symmetric brain lesions

systemic lupus erythematosus

systemic lupus erythematosus, neonatal

systemic lupus erythematosus, neurologic complications with

tachycardia

Tay-Sachs disease

teeth, abnormal

teeth, number of in infants

temper tantrums

temporalis muscle wasting

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

tonic spasms

toxins, nervous system

toxoplasmosis, CNS

tracheostomy

transilumination of skull

treatment of neurologic disorder

tremor

tremor, intention

tremulousness

trinucleotide repeats

type 1 muscle fiber

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

urine test for metabolic disorders

vaccination, neurologic complications with

vision, failure of in childhood

visual evoked response

walking, difficulty with

weakness

weakness, acute

weakness, congenital

weakness, generalized

weakness, infant

weakness, progressive

Werdnig-Hoffman disease

Showing articles 850 to 900 of 1556 << Previous Next >>

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Aggressive Approach in the Treatment of Acute Lead Encephalopathy with an Extraordinarily High Concentration of Lead
Arch Pediatr Adolesc Med 152:1100-1104, Gordon,R.A.,et al, 1998

Ophthalmoplegic Migraine:Reversible Enhancement and Thickening of the Cisternal Segment of the Oculomotor Nerve on Contrast-Enhanced MR Images
AJNR 19:1887-1891, Mark,A.S.,et al, 1998

Long-Term Follow-Up of Levodopa Responsiveness in Generalized Dystonia
Arch Neurol 55:1320-1323, Dewey,R.B.,et al, 1998

Dystonia and Chorea in Acquired Systemic Disorders
JNNP 65:436-445, Janavs,J.L.&Aminoff,M.J., 1998

Incidence of Status Epilepticus in Rochester, Minnesota, 1965-1984
Neurol 50:735-741, Hesdorffer,D.C.,et al, 1998

Clinicopath Conf
Cat Scratch Encephalitis Due to B. Quintana, Case 1-1998, NEJM 338:112-11998., , 1998

Toscana Virus Infections of the Central Nervous System in Children:A Report of 14 Cases
J Pediatr 132:144-148, Braito,A.,et al, 1998

Localization of the Giant Axonal Neuropathy Gene to Chromosome 16q24
Ann Neurol 43:143-148, Flanigan,K.M.,et al, 1998

Spinal Cord Infection:Myelitis and Abscess Formation
AJNR 19:341-348, Murphy,K.J.,et al, 1998

Randomized Prospective Study of Early Discontinuation of Antiepileptic Drugs in Children with epilepsy
Neurol 50:724-730, Peters,A.C.B.,et al, 1998

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

Air Bag-Related Deaths and Serious Injuries in Children:Injury Patterns and Imaging Findings
AJNR 19:1599-1607,1591, Marshall,K.W.,et al, 1998

Subdural Haemorrhages in Infants:Population Based Study
BMJ 317:1558-1561,1538, Jayawant,S.,et al, 1998

Rhabdomyolysis and Hypoxia Associated with Prolonged Propofol Infusion in Children
Neurol 50:301-303, Hanna,J.P.&Ramundo,M.L., 1998

Presentation of Narcolepsy After 40
Neurol 50:459-465, Rye,D.B.,et al, 1998

Evaluation and Management of Intracranial Mass Lesions in AIDS
Rpt of Quality Stnds Subcomm of the AAN, Neurol 50:21-261998., , 1998

Neurologic Outcomes in Children with Post-Pump Choreoathetosis
J Pediatr 132:162-164, Holden,K.R.,et al, 1998

Fibromyalgia Syndrome in Children & Adolescents:Clin Features at Present & Status at Follow-up
Pediatrics 101:377-382, Siegel,D.M.,et al, 1998

Acute Encephalopathy Followeld by Perm Brain Injury or Death Assoc with Further Atten Measles Vaccines
Pediatrics 101:383-387, Weibel,R.E.,et al, 1998

Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 1998

Spastic Diplegia as a Complication of Interferon Alfa-2a Treatment of Hemangiomas of Infancy
J Pediatr 132:527-530, Barlow,C.F.,et al, 1998

MRI of Brain in Very Preterm Infants:Visualization of Germinal Matrix, Early Myelination, & Cortical Foldings
Pediatrics 101:957-962, Battin,M.R.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Clinicopath Conf
Demyelinating Process Consistent with Multiple Sclerosis, Case 26-1998, NEJM 339:542-549998., , 1998

Temporal Lobe Epilepsy in Childhood:Clin, EEG, & Neuroimag Findings & Synd Class in a Cohort with New-Onset Szres
Neurol 49:960-968, Harvey,A.S.,et al, 1998

Magnetic Resonance Imaging Evidence of Hippocampal Injury After Prolonged Focal Febrile Convulsions
Ann Neurol 43:413-426, 4111998., VanLandingham,K.E.,et al, 1998

Long-Term Intellectual and Behavioral Outcomes of Children with Febrile Convulsions
NEJM 338:1723-1728, Verity,C.M.,et al, 1998

Long-Term Prognosis of Seizures with Onset in Childhood
NEJM 338:1715-1722, Sillanpaa,M.,et al, 1998

A Comparison of Rectal Diazepam Gell and Placebo for Acute Repetitive Seizures
NEJM 338:1869-1875, 19161998., Dreifuss,F.E.,et al, 1998

Minimal Head Trauma in Children Revisited:Is Routine Hospitalization Required
Pediatrics 101:575-577, Roddy,S.P.,et al, 1998

Nonaccidental Head Injury in Infants-The"Shaken-Baby Syndrome"
NEJM 338:1822-1829, Duhaime,A-C.,et al, 1998

CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
Neurol 51:844-849, Desmond,D.W.,et al, 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

An Optimality Score for the Neurologic Examination of the Term Newborn
J Pediatr 133:406-416, Dubowitz,L.,et al, 1998

Second Malig in Young Children with Prim Brain Tumors Following Trtm with Prolonged Postop Chemo & Delay Irrad
Ann Neurol 44:313-316, 3001998., Duffner,P.K.,et al, 1998

PCR on CSF to Show Influenza-Associated Acute Encephalopathy or Encephalitis
Lancet 352:873-875, Fujimoto,S.,et al, 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

Prothrombotic Disorders in Infants and Children with Cerebral Thromboembolism
Arch Neurol 55:1539-1543, deVeber,G.,et al, 1998

Anticoagulation Therapy in Pediatric Patients with Sinovenous Thrombosis,A Cohort Study
Arch Neurol 55:1533-1537, deVeber,G.,et al, 1998

Reversal of MR Findings of Central Pontine Myelinolysis
J Comput Assist Tomogr 22:989-991, McGraw,P. & Edwards-Brown,M. K., 1998

Pertussis Encephalopathy with High Cerebrospinal Fluid Antibody Titers to Pertussis Toxin and Filamentous Hemagglutinin
Pediatrics 102:986-990, Grant,C.C.,et al, 1998

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

Risk of Recurrent Seizures After Two Unprovoked Seizures
NEJM 338:429-434, Hauser,W.A.,et al, 1998

Clinical Assessment of Acute Coma in Children
Lancet 351:927-928, Gemke,R.J.B.J.&Tasker,R.C., 1998

Intracranial Penetrating Injuries via the Optic Canal
AJNR 19:1163-1165, Matsumoto,S.,et al, 1998

Prevent of a 1st Stroke by Transfusions in Children/Sickle Cell Anemia & Abnorm Results on Transcr Doppler Ultrasonog
NEJM 339:5-11, Adams,R.J.,et al, 1998

Stroke in Children and Sickle-Cell Disease, Baltimore-Washington Cooperative Young Stroke Study
Neurol 51:169-176, Earley,C.J.,et al, 1998

Clinical Features of Moyamoya Disease in the United States
Stroke 29:1347-1351, Chiu,D.,et al, 1998

Impaired Fetal Growth and Atherosclerosis of Carotid and Peripheral Arteries
Lancet 352:173-178, Martyn,C.N.,et al, 1998

Showing articles 850 to 900 of 1556 << Previous Next >>