Neudle.com: growth failure

Differential
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abdominal distention

abducens nerve paralysis

acetazolamide

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acromicria

adrenal crisis, acute

adverse drug reaction

agenesis of corpus callosum

alcohol

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

algorithm

alopecia

alpha-fetoprotein

alveolar hypoventilation

amyotrophic lateral sclerosis

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

areflexia

arteriovenous malformation

arteriovenous malformation, cerebral

ataxia telangiectasia

atlanto-axial subluxation

attention deficit disorder with hyperactivity

autism

autoimmune disease

autonomic dysfunction

basal ganglia, calcification of

basilar impression

battered child syndrome

behavior modification

behavior, combative

behavioral disorder

biologic markers

bitemporal visual field defect

bone marrow transplantation

brachial plexus neuropathy

brachial plexus neuropathy, familial

Brown-Vialetto-Van Laere syndrome

calcification, intracranial

carbonic anhydrase II deficiency

carcinoembryonic antigen

CAT scan, false negative

cataracts

cavernous sinus

cavernous sinus, metastasis to

celiac disease, adult

celiac disease, childhood

central hypoventilation, congenital

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebral cortex

cerebral cortical atrophy

cerebral palsy

cerebral vasculature

cerebral venous thrombosis

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

chemotherapy, CNS treatment and complications with

chorionic gonadotropin

chorioretinitis

chromophobe adenoma

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

cisterna magna, enlarged

cleft palate

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

coma

complications

compression fracture

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congestive heart failure

Cornelia de Lange syndrome

corpus callosum, atrophy of

corpus callosum, thinning

cortical blindness

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

cryptorchidism

cultured skin fibroblasts

cytochrome c oxidase, deficiency

deafness

degenerative diseases of CNS

dementia

dementia, childhood

dementia, rapidly progressive

dermatitis herpetiformis

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

digits, abnormal

diplopia

dislocated hip, congenital

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

drooling

dural sinus thrombosis

electroencephalogram, abnormalities of

electromyogram

electron microscopy

emergencies, neurologic

empty sella

encephalopathy

encephalopathy, progressive

endovascular therapy

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

eye movement, disorders of

eyebrows, abnormal

eyes, sunken

facial anomalies

facial appearance, abnormal

facial hypoplasia

facial nerve palsy

facial weakness, bilateral

fetal alcohol syndrome

fetus

fever

fibrillations

fine motor function, impaired

finger tapping

floppy infant

foam cells

follicle stimulating hormone

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glucose tolerance test, abnormal

gluten ataxia

gluten sensitivity

gluten-free diet

glycogen debranching enzyme deficiency

glycogen storage disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, infantile and childhood form

head injury, hypothalamic and pituitary damage

head injury, pediatric

hemoglobin abnormality, neurologic complications of

hemorrhage, intracranial, newborn

hemorrhagic diathesis

hepatitis

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary multiple exostoses

herpes simplex virus

herpes simplex virus infection, newborn

herpes simplex virus, human nervous system and

high arched palate

hip dysplasia

Hirschprung's disease

hirsutism

HLA

homocystinuria

human immunodeficiency virus type 1

Hunter's syndrome

hydrocephalus

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, etiology

hydrocephalus, fetal

hydrocephalus, infants and children

hydrocephalus, intrauterine

hydrocephalus, treatment of

hyperpigmentation of skin

hyperreflexia

hypertelorism

hypertonia

hypertrophic cardiomyopathy

hypopigmentation of skin

hypothalamus, disturbance of

hypothalamus, lesion of

hypothalamus, neoplasm of

hypothermia

hypothermia, causes of

iatrogenic neurologic disorders

inability to stand on tiptoes

inclusion bodies, intranuclear

intellectual deterioration

intelligence quotient

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hemorrhage

intracranial hypertension, benign

intracranial hypertension, benign, differential diagnosis

intracranial hypertension, benign, pathogenesis of

intracranial pressure, increased

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

joint hypermobility

Kearns-Sayre syndrome

Klinefelter's syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactate

lactic acidemia

laminar necrosis, cortical

language disorders in children

L-dopa

learning disability, in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

level of consciousness, decreased

libido, decreased

life expectancy

lip, abnormal

lipid storage disorder of CNS

lysosomal storage disease

macrocephaly

malabsorption

malabsorption syndrome

malformation, vascular

malformation, vascular, cerebral

malformation, Vein of Galen

meconium staining

melanomatosis, primary malignant

MELAS syndrome

meningitis, CSF cell count-normal

menses

mental retardation

mental status, abnormal

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

molybdenum cofactor deficiency

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRS

mucopolysaccharidoses

multiple sclerosis

multiple system atrophy

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelination of nervous system

myoclonus, stimulus sensitive

myopathy

myopathy, distal

myopathy, distal, vacuolar

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

neoplasm, intracranial with metastasis extracranially

neoplasm, intracranial, congenital

neoplasm, intracranial, infants

neoplasm, pituitary

neoplasm, primary intracranial

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve growth factor

nerve growth stimulating activity

neuroblastoma

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory, hereditary

neuroprotective agents

nutritional deficiency

nystagmus

nystagmus, see-saw

obesity

ocular motility, disorders of

oligodactyly

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

optic atrophy

optic foramina

optic foramina, abnormal

optic nerve sheath fenestration

optic nerve, decompression of

optic nerve, hypoplasia of

optic neuropathy

oral ulcerations

orthostatic hypotension, idiopathic

osteogenesis imperfecta

Pallister-Hall syndrome

palpebral fissure, short

pancytopenia

papilledema

paraparesis

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinson disease, differential diagnosis of

Parkinsonism syndrome

parotitis

paroxysmal neurologic deficits

PAS positive

patent ductus arteriosus

perceptual-motor dysfunction

personality change

pheochromocytoma

philtrum, hypoplastic

phocomelia

photophobia

photosensitivity, skin

pigmentary retinopathy

pinched face

pitfalls

pituitary, adenoma

pituitary, dysfunction

pituitary, enlargement

pituitary, hormones of

pituitary, lesion of

PLEDs

PLEDs, bilateral independent

PLEDs, etiology of

polydactyly

polyhydramnios

polyps, gastrointestinal tract

pons, atrophy

postural abnormality

Prader-Labhart-Willi syndrome

precocious puberty

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primitive neuroectodermal tumors

progeria

prognathism

prognosis

progressive neurologic disorder

proteinuria

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pupil, ectopic-congenital

pyramidal tract dysfunction

quadriparesis

quadriplegia

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

rash

reading problem, causes of

recurrent

renal failure

renal tubular acidosis

respirations in CNS disease

respirator

respiratory failure

respiratory tract infection

riboflavin transporter deficiency

Schwartz-Jampel syndrome

sclerae, blue

scoliosis

scoliosis, neurologic association with

screaming

seizure

seizure, children

seizure, drug resistance

seizure, focal

seizure, injury following

seizure, intractable

seizure, neonatal

sella turcica, enlargement of

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

serologic testing

short neck

short stature

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

sleep

sleep pathology and physiology

small vessel disease

somatosensory evoked potentials

spastic diplegia

spasticity

speech disorder

speech disorder, childhood

speech, delayed development of

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

splenomegaly

spongy degeneration of brain

standing difficulty

stem cell transplantation

subarachnoid hemorrhage

subdural hematoma

subdural hematoma, neonates and infants

subgaleal fluid collection

suck, poor

superior sagittal sinus thrombosis

temporal lobe, lesion

teratoma

term infant

third ventricle, mass of

thyroid function tests

toe walking

tongue, enlarged

tongue, protrusion of

transplacental virus infections

treatment of neurologic disorder

urea-cycle enzymopathies

uric acid, low

urinary 17 hydroxycorticosteroids

urinary 17 ketosteroids

valvulopathy

vein of Galen

ventriculostomy, endoscopic

viral infection, CNS

visual acuity, decreased

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

x-linked mental retardation

x-ray, cervical spine

Showing articles 50 to 100 of 1827 << Previous Next >>

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

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

Reversible Suprasellar Pituitary Mass Secondary to Hypothyroidism
JAMA 262:3175, 31771989., Atchison,J.A.,et al, 1989

Congenital AIDS:Review of Neurological Problems
Child's Nerv Syst 5:9-11, Curles,R.G., 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

Myopathy and Cystine Storage in Muscles in a Patient with Nephropathic Cystinosis
NEJM 392:1461-1464, Gahl,W.A.,et al, 1988

Diagnostic Criteria for Rett Syndrome
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MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

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

Natural History of the Fetal Alcohol Syndrome:A 10-Year Follow-Up of Eleven Patients
Lancet 2:85-91, Streissguth,A.P.,et al, 1985

Mitochondrial Myopathies
Ann Neurol 17:521-538, DiMauro,S.,et al, 1985

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

Precocious Puberty after Hypothalamic & Pituitary Irradiation in Young Children
NEJM 311:920-921, Brauner,R.,et al, 1984

Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome
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Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Ultrastructure & Electrodiagnosis of Peripheral Neuropathy in Cockayne's Syndrome
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Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease
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Child Abuse as a Cause of Post-Traumatic Hypopituitarism
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Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

Paraparesis in Hereditary Multiple Exostoses:Case Report
Neurol 29:973-977, Ferrari,G.,et al, 1979

Intracranial Arteriovenous Malformations in Childhood
Ann Neurol 3:338, Kelly,J.J.,et al, 1978

A Syndrome of Progressive Muscle Spasm, Alopecia, & Diarrhea
Neurol 28:458, Satoyoshi,E., 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

Familial Hypopituitarism with Large Sella Turcica
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A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
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Growth & Development in Children with Sickle-Cell Trait
NEJM 299:686-689, Kramer,M.S.,et al, 1978

Nerve Growth Factor (three parts)
NEJM 297:1096, 1149, 1211977., Mobley,W.C.,et al, 1977

Chronic Hydrocephalus Associated with Short Stature & Growth Hormone Deficiency
Ann Neurol 2:246, Hier,D.B.,et al, 1977

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

Nerve-Growth Factor in Familial Dysautonomia
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Germinoma of third Ventricle (Case Record of MGH)
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A Comparison of the Physical & Intellectual Development of Black Children with & without Sickle-Cell Trait
Pediatrics 56:1021, McCormack,M.K.,et al, 1975

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

Treating Problem Children with Stimulant Drugs
NEJM 289:407, Sroufe,L.A.,et al, 1973

Congenital Anomalies & Herpesvirus Infection
Am J Dis Child 126:364, Montogomery,J.R.,et al, 1973

Depression of Growth in Hyperactive Children on Stimulant Drugs
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Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
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The Mucopolysaccharidoses
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Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith
W. B. , Saunders Co. , 1970, 248-249., David,W., 1970

Endocrine Function in Patients with Untreated Chromophobe Adenomas
Quart J Med 357, Neiman,E.A.,et al, 1968

Morquio's Disease, A Radiologic & Morphologic Study
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