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 50 to 100 of 1571 << Previous Next >>

Transsection of the Spinal Cord Associated with Breech Delivery
Am J Dis Child 146:351-352, DiMario,F.J.&Wood,B.P., 1992

Neonatal Idiopathic Cerebral Venous Thrombosis:An Unrecognized Cause of Transient Seizures or Lethargy
Ann Neurol 32:51-56, Rivkin,M.J.,et al, 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Long-Term Neurologic Consequences of Nutritional Vitamin B12 Deficiency in Infants
J Pediatr 121:710-714, Graham,S.M.,et al, 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Infant Botulism:A Review of 12 Years'Experience at the Children; s Hosp of Phila
Pediatrics 87:159-165, Schreiner,M.S.,et al, 1991

Neonatal Lupus Erythematosus Simulating Transient Myasthenia Gravis at Presentation
J Pediatr 118:417-419, Rider,L.G.,et al, 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
Clin genet 37:355-362, Clarke,J.T.,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

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

The Causes of Cerebral Palsy
JAMA 247:1473-1477, Holm,V.A., 1982

Clin. Path. Conference
Osteopetrosis, Malignant Juvenile Form, Case Record 37-1982, NEJM 307:735-74382., , 1982

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Subgaleal Hematoma, A Complication of Instrumental Delivery
JAMA 244:1597-1598, Plauche,W.C., 1980

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Intracranial Hemorrhage in the Newborn:Current Understanding & Dilemmas
Neurol 29:632-635, Volpe,J.J., 1979

Hyperphenylalaninemia Due To A Deficiency of Biopterin
NEJM 299:673-679, Stanley,S.K.,et al, 1978

Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,et al, 1978

A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
NEJM 299:317, Higginbottom,M.C., 1978

The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

Neonatal Ophthalmoplegia with Microfibers:A Reversible Myopathy
Neurol 27:974, Hanson,P.A.,et al, 1977

Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
Arch Neurol 34:567, Gilmartin,R.C.,et al, 1977

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

Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972

The Hypotonic Infant
Med Progress 64:422, Rabe,E., 1964

Neuro CPC of MGH
Congenital Toxoplasmosis Involving CNS, NEJM 269:369-3741963., , 1963

Neurology & Psychiatry Section-Year book of Pediatrics
Pediatr Abstract p. 406-449., , 1850

A 5-Year-Old Boy with Subacute and Refractory Myoclonus
Neurol 106:e214457, Park,P.S.,et al, 2025

Spontaneous Intracranial Hypotension Associated with Vascular Malformations
AJNR 46:426-432, Mamlouk,M.D.,et al, 2025

Dextromethorphan-Associated Neurotoxicity with Cerebellar Edema Syndrome in Young Children:Neuroimaging Features
AJNR 46:390-394, Sharma,S.,et al, 2025

Polka Dot Intracerebral Hemorrhage in Leukemia
Stroke 56:e49-e50, Rebchuk,A.D.,et al, 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

Bobble-Head Doll Syndrome in a Child
Neurol 104: e213694, Chityala,A.,et al, 2025

SWI Filtered-Phase Imaging in Basal Ganglia Stroke Caused by Mineralizing Angiopathy of Childhood
Neurol 105: e213730, Bektas,G.,et al, 2025

The Spectrum of Fragile X Disorders
NEJM 393:281-288, Hagerman,R.H. & Hagerman,P.J., 2025

A 2-Year-Old Girl with Acute Encephalopathy After Febrile Systemic Illness
Neurol 105:e213970, Westendfortp,W.F.,et al, 2025

Risdiplam in Presymptomatic Spinal Muscular Atrophy
NEJM 393:671-682, Finkel,R.S.,et al, 2025

A 9-Year-Old Girl with CNS Immune Dysregulation
Neurol 105:e213999, Marefi,A.,et al, 2025

Neuroimaging Findings in Children and Young Adults with Neurotoxicity after CAR T-Cell Therapy for B-Cell Malignancies
Neurol 105:e214086, McGuire,J.L.,et al, 2025

A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
Neurol 105:e214297, Chen,Z., et al, 2025

Multivessel Cerebral Occlusion in Noonan Syndrome
Stroke 56:e359-362, deLima, M.M.,et al, 2025

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Showing articles 50 to 100 of 1571 << Previous Next >>