Neudle.com: "hepatomegaly"

Differential
(Click to cross reference)

abducens nerve paralysis

abscess, brainstem

abscess, intracerebral

abscess, intracranial

abscess, lung

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acyl CoA dehydrogenase deficiency

Addison's disease

adrenoleukodystrophy

adverse drug reaction

altered states of consciousness

aneurysm, abdominal aortic

aneurysm, aortic arch

aneurysm, intracranial

aneurysm, vertebral basilar system

angiitis

angioimmunoblastic lymphadenopathy

anterior horn cell disease

anti DNA agent

antibiotics, neurologic complications with

anticonvulsants

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

aspartate aminotransferase

ataxia telangiectasia

Babinski sign in new born

basal ganglia, calcification of

basal ganglia, lesion of

basophilia

basophilic stippling of red blood cells

bone density, increased

bone marrow biopsy

bone marrow transplantation

bone pain

bone survey

bone survey, metastatic

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

breast feeding

brucellosis

brucellosis, nervous system involvement with

burning paresthesia

cachexia

calcification, intracranial

calf hypertrophy

California

cancer, cerebrovascular accident complicating patients with

candida albicans

carbamazepine

carbamazepine, toxicity

carcinoma

carcinoma of bladder

carcinoma of liver

carcinoma of pancreas

cardiomegaly

cardiomyopathy

carnitine deficiency

carnitine deficiency myopathy

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

CAT scan, emission, abnormal

cataplexy

cataracts

cataracts, congenital

cat-scratch disease

CD4 counts

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

central retinal artery occlusion

cerebellar infarction

cerebellum, disease of

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral infarction

cerebral infarction, hemorrhagic

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, protein of

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

ceruloplasmin, serum

Chediak-Higashi syndrome

chemosis

chemotherapy, CNS treatment and complications with

cherry red spot

chest x-ray, abnormal

chromosomal abnormality

chronic graft versus host disease

Churg-Strauss syndrome

cirrhosis

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

color vision, impaired

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital paresis

congestive heart failure

conjunctivitis

consanguinity

contractures, joint

Coombs test, positive

copper metabolism, abnormal

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

cotton-wool spots

cough

cranial nerve palsies

cranial neuropathy, multiple

crawl regression

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

crying, pathologic

cryptococcal meningitis

cryptococcosis

cryptorchidism

cultured skin fibroblasts

cyanosis

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

degenerative diseases of CNS

delirium

dementia

dementia, childhood

demyelinating disease

Dengue fever

depression

dermatitis

dermatitis herpetiformis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

dialysis

diaphragmatic paralysis

diarrhea

differential diagnosis

DiGeorge syndrome

diplopia

disability, neurological

distal muscle atrophy

downward gaze, paralysis of

echocardiogram, transesophageal

echocardiogram, transthoracic

edema, facial

edema, pedal

edema, periorbital

EDTA(ehtylenediamine tetraacetic acid)

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram

electron microscopy

electrophoretic pattern, serum

endocarditis, marantic

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilia-myalgia syndrome

epidemiology of neurology

episodic disorders

episodic neurologic deficits

epistaxis

Epstein-Barr virus

Epstein-Barr virus, negative

erythema nodosum

erythroderma

esophageal varices

exercise-induced neurologic dysfunction

eye movement, disorders of

eye, pain in

face, numbness of

facial anomalies

facial appearance, abnormal

fatty acid, elevated plasma content

fistula, arterio-venous, pulmonary

flea bite

fleas

fluctuate

fluorescent treponema antibody absorption/false positive

fundus, abnormality of

fungal infection, CNS

gastrointestinal bleeding

Gaucher's disease

Gaucher's disease, adult onset

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glycogen debranching enzyme deficiency

glycogen storage disease

glycoprotein

granulomatosis with polyangiitis

granulomatosis, allergic

granulomatous disease

Guillain Barre syndrome

hallucination, visual

Hand-Schuller-Christian disease

headache, retro-orbital

hematuria, microscopic

hemianopia, homonymous

hemiparesis

hemiplegia

hemoglobin abnormality, neurologic complications of

hemolytic-uremic syndrome

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemoptysis

hemorrhagic diathesis

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatitis

hepatitis E virus

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), late onset

hepatolenticular degeneration(Wilson's disease), screening for

hepatoma

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herpes virus infection

heterophile antibody test

highly active antiretroviral therapy

hirsutism

histoplasmosis

Horner's syndrome

human immunodeficiency virus type 1

Hunter's syndrome

Hurler's syndrome

hydrocephalus

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hyperbilirubinemia

hypercalcemia

hypercoagulable state

hypereosinophilic syndrome(HES)

hyperesthesia

hypergammaglobulinemia

hyperhidrosis

hyperphosphatasia

hyperpigmentation of skin

hyperreflexia

hypersensitivity reaction

hypertrophic cardiomyopathy

hyperviscosity

hyperviscosity syndrome

hypofibrinogenemia

hypogammaglobulinemia

hypoglycemia

hypoglycorrhachia

hypogonadism

hypopigmentation of skin

hyporeflexia

hypothalamus, disturbance of

hypothyroidism

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

IFA

immune reconstitution inflammatory syndrome

immune reconstitution inflammatory syndrome, paradoxical

immune reconstitution inflammatory syndrome, unmasked

immunodeficiency

immunoelectrophoresis, serum

inborn errors of metabolism

inclusion bodies

incoordination

increased intracranial venous pressure

infection

infection, recurrent

infectious mononucleosis

insect sting

intellectual deficit

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia, unilateral

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrathecal medication

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

Kayser-Fleischer ring

keratitis

keratitis, interstitial

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

lacunar infarction

lead and the nervous system

lead poisoning

learning disability, in children

leukemia, neurologic findings assoc.with

leukocytosis

leukopenia

level of consciousness, decreased

life expectancy

lipid storage disorder of CNS

lipid storage myopathy

livedo reticularis

liver biopsy

liver disease

liver function enzymes

liver transplantation

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphadenopathy, paraaortic

lymphocytic interstitial pneumonitis

lymphoma involving CNS

lymphomatoid granulomatosis

lysosomal storage disease

malformation, vascular

malformation, vascular, cerebral

malignant histiocytosis

mastoiditis

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, chronic

meningitis, eosinophilic

meningitis, fungal

meningitis, histoplasma

meningitis, leptospira

meningitis, Mollaret's

meningitis, recurrent

meningitis, TB

meningoencephalitis

mental retardation

mental status, abnormal

metabolic acidosis

metachromatic leukodystrophy

microcephaly

micropthalmia

migraine, seizures in

misdiagnosis

mitral valve lesion

mitral valve vegetation

MNGIE syndrome

mongolism

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

mortality

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

mucopolysaccharidoses

mucopolysacchariduria

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myasthenia gravis

mycobacterial infection

mycobacterium bovis

mycoplasma

mycoplasma pneumoniae

mycotic aneurysm

myelitis

myeloma, osteosclerotic

nasal septum, perforation of

neonatal infection, viral

neoplasm, metastatic to base of skull

neoplasm, metastatic to CNS

neoplasm, metastatic to Dura

neoplasm, primary of CNS

nerve biopsy

neuroendocrinology

neurofibrillary degeneration

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, vasculitic, systemic

nutritional deficiency

nystagmus

nystagmus, dissociated

nystagmus, rotary

nystagmus, vertical

occupational neurologic disorders

ocular motility, disorders of

opened mouth

ophthalmoplegia

opisthotonus

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic atrophy, infants

optic neuritis

optokinetic nystagmus, abnormal

organomegaly

orthopnea

osteolytic lesion, causes of

osteopetrosis

otitis, neurologic complications with

parasitic infection, CNS

paresthesias

Parkinsonism syndrome

parotitis

PAS positive

PAS positive material in the brain

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

pituitary stalk, lesion of

pituitary, enlargement

pituitary, lesion of

plasmacytoma

plasmapheresis

pleocytosis of cerebrospinal fluid

polycythemia, primary

polycythemia, secondary

polyhydramnios

polymerase chain reaction

polymyositis

polymyositis, eosinophilic

polyneuropathy

Pompe's disease of glycogen storage

portal caval shunt

post infectious polyneuropathy

posterior inferior cerebellar artery syndrome

postpartum

postpartum coma

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary thrombocythemia

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

prolactin, elevated

prothrombin time, prolonged

protozoan infection

pruritus

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis

ptosis

pulmonary function tests

pulmonary infiltrates

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia

quadriplegia, transient

radiation therapy, CNS treatment and complications with

respiratory tract infection

retinal artery occlusion

rheumatic heart disease

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rubella encephalitis, progressive

salivation, excessive

scoliosis, neurologic association with

scotoma

sedimentation rate, elevated

seizure

seizure, children

seizure, focal

seizure, injury following

seizure, laughing as manifestation

seizure, neonatal

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

serositis

serum alanine aminotransferase

skin, lesions in neurologic disorders

skin, thickened

skull x-ray

skull x-ray, abnormal

skull, metastatic carcinoma to

sleeping sickness

slow virus infection of CNS

small for dates infant, problems in

sore throat

spasticity

speech, delayed development of

speech, loss of

sphingolipodoses

spinal cord, compression of

spinal cord, infarction of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal cord, vascular malformation of

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

stiff joints

striatonigral degeneration

striatonigral degeneration, infantile

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

subarachnoid hemorrhage

symmetric brain lesions

systemic illness

systemic juvenile idiopathic arthritis

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

systemic lupus erythematosus, skin changes in

tachycardia

Tangier's disease

telangiectases

telangiectases, retinal

thrombotic thrombocytopenia purpura

transient ischemic attack

transilumination of skull

transplacental virus infections

travel history

travel, foreign

treatment of neurologic disorder

tremor

tremor, intention

tremor, wing beating

trigeminal neuropathy

trigeminal neuropathy, sensory

tropical disease

Trousseau's syndrome

trypanosoma brucei gambiense

tsetse fly

tuberculosis

typhus, murine

ultrasonography, head

upgaze

upgaze, paralysis of

uremia

urine test for metabolic disorders

urticaria

uveitis

valvulopathy

vascular endothelial growth factor

vascular headache, food causing

vasculitides

vasculopathy

vectors of infection

Venereal Disease Research Laboratory test

vertebral erosion

vertigo

vincristine neurotoxicity

viral infection

viral infection, CNS

viral isolation

Virchow-Robin spaces, dilated

virus, slow

vision, blurred

visual acuity, decreased

visual evoked response

Vogt-Koyanagi-Harada syndrome

vomiting, recurrent

Waldenstrom's macroglobulinemia

walking, difficulty with

weakness

weakness, episodic

weakness, fluctuating

weakness, generalized

weakness, progressive

Wiskott-Aldrich syndrome

workup

writing

x-ray, lumbar spine

Showing articles 0 to 50 of 104 Next >>

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Babesiosis: Clinical Manifgestations and Diagnosis
www.UptoDate.com, Oct, Krause,P.J. & Vannier,E.G., 2022

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

Clinicopathologic Conference, Disseminated Mycobacterium Bovis Infection
NEJM 384:651-662, Case 5-2021, 2021

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

A Headache of a Diagnosis
NEJM 379:475-479, Stern,R.M.,et al, 2018

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

Two Uncommon Causes of Guillain-Barr� Syndrome: Hepatitis E and Japanese Encephalitis
Case Reports Neurol Med Art ID:759495, Bandyopadhyay, D.,et al, 2015

Hepatitis Associated with Mycoplasma Pneumoniae Infection in Korean Children:A Prospective Study
Korean J Pediatr 58:211-217, Kim,K.W.,et al, 2015

Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
NEJM 370:911-920, Zhou, Q.,et al, 2014

Griscelli Syndrome and CNS Lymphohistiocytosis
Neurol 82:e122-e123, Saini, A.G.,et al, 2014

Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
UptoDate Oct. 2014, McClain, K.L., 2014

Inherited Metabolic Diseases of the Nervous System, Infantile Niemann-Pick Disease
Adams & Victors Principles of Neurology, Chp 37, pg 958, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 982, Ropper, A.H.,et al, 2014

Chediak-Higashi Syndrome: Pathognomonic Feature
Lancet 382:1514, Antunes, H.,et al, 2013

CNS-Immune Reconstitution Inflammatory Syndrome in the Setting of HIV Infection, Part 1: Overview and Discussion of Progressive Multifocal Leukoencephalopathy-Immune Reconstitution Inflammatory Syndrome and Cryptococcal-Immune Reconstitution Inflammatory Syndrome
AJNR 34:1297-1307, Post, M.J.D.,et al, 2013

Epidemiology, Pathogenesis, Clinical Manifestations and Diagnosis of Waldenstrom Macroglobulinemia
UptoDate, May, Rajkumar, S.V., 2011

Infectious Mononucleosis in Adults and Adolescents
UpToDate, May, Aronson,M.D. & Auwaerter,P.G., 2011

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Cogan Syndrome
www.medlink.com, Feb, Ramachandran, T.S., 2010

A Case of Acute Hepatitis with Mycoplasma Pneumoniae Infection and Transient Depression of Multiple Coagulation Factors
Yonsei Med J 49:1055-1059, Chang, J.H.,et al, 2008

Liver Involvement in Celiac Disease
Minerva Med 99:595-604, Rubio-Tapia,A. & Murray,J.A., 2008

Lethal African Trypanosomiasis in a Traveler: MRI and Neuropathology
Neurol 66:1094-1096,962, Braakman,H.M.H.,et al, 2006

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

POEMS Syndrome Associated with Ischemic Stroke
Arch Neurol 60:745-749, Kang, K.,et al, 2003

Clinicopath Conf., Adenocarcinoma with Metastasis to Liver, with Hypercoagulable State Resulting in Thrombophlebitis & Nonbacterial Thrombotic Endocarditis, with Multiple Embolic Infarcts (Trousseau's
NEJM 347:1187-1194, Case 31-2002, 2002

A Tourist With Dengue Fever and Visual Loss
Lancet 360:1070, Haritoglou,C.,et al, 2002

MR Brain Imaging of Fucosidosis Type I
AJNR 22:777-780, Galluzzi,P.,et al, 2001

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Postpartum Coma
Lancet 351:1700, McCormack,G.,et al, 1998

An Anaemic Infant in a Coma
Lancet 352:284, Kokori,H.,et al, 1998

Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
J Pediatr 133:119-125, 71998., Guffon,N.,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

Thrombotic Thrombocytopenic Purpura:A Treatable Cause of Childhood Encephalopathy
J Pediatr 130:313-316, Lawlor,E.R.,et al, 1997

An Emotional 13-Year Old Girl
Lancet 348:1000, Kanabar,D.J.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Carbamazepine Hypersensitivity Syndrome:Report of 4 Cases & Review of Literature
Medicine 74:144-151, DeVriese,A.S.P.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

POEMS Syndrome:A Study of 25 Cases and a Review of the Literature
Am J Med 97:543-553, Soubrier,M.J.,et al, 1994

Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
J Pediatr 123:242-247, Kelly,D.A.,et al, 1993

Neimann-Pick Disease Type C in a Middle-Aged Woman
Neurol 43:1435-1436, Lanska,D.J.&Lanska,M.J., 1993

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Clinicopath Conf
PEOMS Syndrome, Case 39-1992, NEJM 327:1014-1021992., , 1992

Hepatoma Presenting as Carniospinal Metastasis:Analysis of Sixteen Cases
JNNP 55:1037-1039, Lee,J., 1992

Showing articles 0 to 50 of 104 Next >>