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

Showing articles 850 to 900 of 1520 << Previous Next >>

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Dystonia and Chorea in Acquired Systemic Disorders
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Incidence of Status Epilepticus in Rochester, Minnesota, 1965-1984
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Spinal Cord Infection:Myelitis and Abscess Formation
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Randomized Prospective Study of Early Discontinuation of Antiepileptic Drugs in Children with epilepsy
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Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
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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
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Mucolipidosis Type IV; Characteristic MRI Findings
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Clinicopath Conf
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Temporal Lobe Epilepsy in Childhood:Clin, EEG, & Neuroimag Findings & Synd Class in a Cohort with New-Onset Szres
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Magnetic Resonance Imaging Evidence of Hippocampal Injury After Prolonged Focal Febrile Convulsions
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Long-Term Intellectual and Behavioral Outcomes of Children with Febrile Convulsions
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Long-Term Prognosis of Seizures with Onset in Childhood
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A Comparison of Rectal Diazepam Gell and Placebo for Acute Repetitive Seizures
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Minimal Head Trauma in Children Revisited:Is Routine Hospitalization Required
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Nonaccidental Head Injury in Infants-The"Shaken-Baby Syndrome"
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CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
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Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
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An Optimality Score for the Neurologic Examination of the Term Newborn
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Second Malig in Young Children with Prim Brain Tumors Following Trtm with Prolonged Postop Chemo & Delay Irrad
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PCR on CSF to Show Influenza-Associated Acute Encephalopathy or Encephalitis
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Inherited Prothrombotic States and Ischaemic Stroke in Childhood
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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

Subdural Haemorrhages in Infants:Population Based Study
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Evaluation and Management of Intracranial Mass Lesions in AIDS
Rpt of Quality Stnds Subcomm of the AAN, Neurol 50:21-261998., , 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
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Rhabdomyolysis and Hypoxia Associated with Prolonged Propofol Infusion in Children
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Neurologic Outcomes in Children with Post-Pump Choreoathetosis
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Fibromyalgia Syndrome in Children & Adolescents:Clin Features at Present & Status at Follow-up
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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

Risk of Recurrent Seizures After Two Unprovoked Seizures
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Clinical Assessment of Acute Coma in Children
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Intracranial Penetrating Injuries via the Optic Canal
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Prevent of a 1st Stroke by Transfusions in Children/Sickle Cell Anemia & Abnorm Results on Transcr Doppler Ultrasonog
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Stroke in Children and Sickle-Cell Disease, Baltimore-Washington Cooperative Young Stroke Study
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Clinical Features of Moyamoya Disease in the United States
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Impaired Fetal Growth and Atherosclerosis of Carotid and Peripheral Arteries
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Tourette Syndrome:Update and Review of the Literature
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Childhood Onset of Benign Positional Vertigo
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Cerebral Aneurysmal Arteriopathy in Childhood AIDS
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Pitfalls in the Diagnosis of Ventricular Shunt Dysfunction:Radiology Reports and Ventricular Size
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Neurological Manifestations of Falciparum Malaria
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Showing articles 850 to 900 of 1520 << Previous Next >>