Neudle.com: floppy infant

Differential
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abdominal distention

acetylcholine receptor antibody

acid maltase deficiency

acromicria

adverse drug reaction

anemia, megaloblastic

Angelman syndrome

angiokeratoma

anorexia

anterior horn cell disease

arthrogryposis multiplex

attention deficit disorder with hyperactivity

autonomic dysfunction

B 12 deficiency

B 12 deficiency, infants

Babinski sign in new born

bacterial infection

basal ganglia, lesion, bilateral

bone marrow transplantation

botulinum toxin

botulism

botulism antitoxin

botulism immune globulin

bulbar palsy, childhood

calcification, intracranial

celiac disease, childhood

central core disease

central nervous system, infection of

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebral cortical atrophy

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, protein of

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

chromosomal abnormality

chromosome 1

chromosome 15

chromosome 5

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

coma

congenital heart disease

congenital infection, CNS

congenital infection, viral

congenital myopathy

congenital myopathy, inflammatory

corpus callosum, thinning

Craniosynostosis

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

delivery, complicated

dementia

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diet

differential diagnosis

diphtheria-tetanus-pertussis immunization

dislocated hip, congenital

electroencephalogram, abnormalities of

electromyogram

electron microscopy

embolism, paradoxical

encephalitis

encephalomyelitis

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

enzyme, defect

epidemiology of neurology

exome sequencing

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

fetal movements, reduced

gammaglobulin therapy, intravenous

gene

gene mutation

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

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

histochemistry of muscle

Horner's syndrome, bilateral

Horner's syndrome, congenital

human genome

Hunter's syndrome

hydrocephalus

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperphagia

hyperpigmentation of skin

hypogammaglobulinemia

hypogonadism

hypokinesia

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

intestinal biopsy

intracranial hemorrhage

intracranial pressure, increased

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

kyphoscoliosis, neurologic causes of

listeria monocytogenes

liver function enzymes

lysosomal storage disease

macrocephaly

malabsorption

malformation, CNS, congenital

malformation, vascular

malignant hyperpyrexia

McArdle's disease

mental retardation

merosin

metabolic disorder, primary

microcephaly

micrognathia

micropthalmia

migraine, seizures in

misdiagnosis

mitochondrial disease

mitral valve prolapse

mucopolysaccharidoses

mucopolysacchariduria

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle diseases, characteristics of

muscle phosphorylase deficiency

muscle weakness

muscle weakness, proximal

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

myelomalacia

myoclonic jerks

myopathy

myopathy, centronuclear

nemaline rod myopathy

neonatal infection, viral

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

nerve conduction studies

nerve conduction studies, motor

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal migration disorder

neuropathology

neuropathology, brain

neurotoxin

newborn, evaluation of

nusinersen

nystagmus

obesity

obstetric neurologic injuries

opened mouth

ophthalmoplegia

ophthalmoplegia, neonatal

ophthalmoplegia, total

optic atrophy

pachygyria

pathology

patient information and support

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

polymerase chain reaction

polymicrogyria

polymyositis

polymyositis, infantile

postpartum

Prader-Labhart-Willi syndrome

precocious puberty

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prognosis

progressive neurologic disorder

psychomotor retardation

reflex, tonic stretch

respirator

respiratory arrest

respiratory depression

respiratory distress syndrome, neurologic status with

scoliosis, neurologic association with

screaming

screening

segmental demyelination

sensorineural hearing loss

serum alanine aminotransferase

short stature

shunt procedure, ventricular

skin, biopsy

skin, lesions in neurologic disorders

small for dates infant, problems in

SMN1 gene

spastic diplegia

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

systemic lupus erythematosus

systemic lupus erythematosus, neonatal

systemic lupus erythematosus, neurologic complications with

tachycardia

temper tantrums

temporalis muscle wasting

tongue, fasciculations of

tongue, protrusion of

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, head

urine test for metabolic disorders

vaccination, neurologic complications with

walking, difficulty with

weakness

weakness, congenital

weakness, generalized

weakness, infant

weakness, progressive

Werdnig-Hoffman disease

white matter disease

wide based gait

workup

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Showing articles 600 to 650 of 1507 << Previous Next >>