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Differential
(Click to cross reference)
attention deficit disorder with hyperactivity
cost effectiveness
DNA probes
ear, abnormal
face, elongated
facial appearance, abnormal
familial
fragile-X syndrome
genetic counselling
genetic diagnosis, prenatal
genetic screening
genetic testing
hyperactivity
joint hypermobility
Kearns-Sayre syndrome
mental retardation
mental retardation, familial
mitochondrial disease
myopathy, mitochondrial
neurologic disease, diagnoses of
ocular myopathy
ophthalmoplegia
ophthalmoplegia, progressive external
prenatal diagnosis by amniocentesis
simian crease
Southern immunoblot test
testicular enlargement
Showing articles 0 to 26 of 26

A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
NEJM 325:1673-1681, Rousseau,F.,et al, 1991

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Brainstem Abnormalities and Vestibular Nerve Enhancement in Acute Neuroborreliosis
BMC Res Notes 6:551, Farshad-Amacker,N.A.,et al, 2013

Clinicopath Conf, Acute HIV-1 Infection
NEJM 360:1540-1548, Case 11-2009, 2009

Clinicopath Conf,Lyme Disease of the Nervous System
NEJM 356:1561-1570, Case Record 11-2007, 2007

Polymerase Chain Reaction Analysis and Oligoclonal Antibody in the Cerebrospinal Fluid From 34 Patients With Varicella-Zoster Virus Infection of the Nervous System
JNNP 77:938-942, Gregoire,S.M.,et al, 2006

Lyme Neuroborreliosis Presenting as the Syndrome of Inappropriate Antidiutetic Hormone Secretion
MedGenMed 8:71, Perkins, M.P.,et al, 2006

Central Nervous System Infection in Congenital Syphilis
NEJM 346:1792-1798, Michelow,I.C.,et al, 2002

A Rash, Circulating Anticoagulant, Then Meningitis
Lancet 351:1856, Schanen,A.,et al, 1998

Detection of 14-3-3 Protein in Cerebrospinal Fluid Supports Dx of Creutzfeldt-Jakob Disease
Ann Neurol 43:32-40, Zerr,I.,et al, 1998

Laboratory Evaluation in the Diagnosis of Lyme Disease
Ann Int Med 127:1109-1123, 1106-11081997., Tugwell,P.,et al, 1997

CSF Findings in Children with Lyme Disease-Associated Facial Nerve Palsy
Arch Pediatr Adolesc Med 151:1224-1228, 11831997., Belman,A.L.,et al, 1997

Diagnostic Value of CSF Exam in Children with Peripheral Facial Palsy & Suspected Lyme Borreliosis
Neurol 49:817-824, Albisetti,M.,et al, 1997

X-Linked Emery-Dreifuss Muscular Dystrophy Can Be Diagnosed from Skin Biopsy or Blood Sample
Ann Neurol 42:249-253, Mora,M.,et al, 1997

Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease
Arch Neurol 53:913-920, Kretzschmar,H.A.,et al, 1996

Detection of Borrelia Burgdorferi-Specific Antigen in Antibody-Negative Cerebrospinal Fluid in Neurologic Lyme Disease
Neurol 45:2010-2015, Coyle,P.K.,et al, 1995

Isolation of HTLV-II from Pt with Chronic, Prog Neurol Dis Clin Indistinguish from HAM/Tropical Spastic Paraparesis
Ann Neurol 33:392-396, Jacobson,S.,et al, 1993

Nervous System Lyme Borreliosis-Revisited
Arch Neurol 49:102-107, Finkel,M.J.&Halperin,J.J., 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

The Widening Spectrum of Infectious Neurological Disease
JNNP 53:629-632, Kennedy,P.G., 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Clinicopath Conf
Lyme Disease, Case Record 51-1988, NEJM 319:1654-1662988., , 1988

Chronic Progressive Myelopathy Associated with Elevated Antibodies to HTLV-I & Adult T-Cell Leukemialike Cells
Ann Neurol 21:117-121, Osame,M.,et al, 1987

Association Between Lupus Psychosis & Anti-Ribosomal P Protein Antibodies
NEJM 317:265-271, 3091987., Bonfa,E.,et al, 1987

Diagnosis of Creutzfeldt-Jakob Disease by Western Blot Identification of Marker Protein in Human Brain Tissue
NEJM 314:547-551, Brown,P.,et al, 1986



Showing articles 0 to 26 of 26