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Showing articles 0 to 29 of 29

Filter Applied: hemoglobin abnormality,neurologic complications of (Click to remove)

Sickle Cell Trait & Central Retinal Artery Occlusion
Am J Ophthalmol 63:465, Conrad,W.C.,et al, 1967

Abnormal Hemoglobin as a Cause of Neurolic Disease
Neurol 12:114, Greer,M.,et al, 1962

A Case of Fulminant Encephalopathy in a 69-year-old Woman
Neurol 89:e109-e114, Lamotte, G. and Williams, C, 2017

Clinicopathologic Conference, Cerebral Infarction from Internal Carotid Occlusion Related to Sickle Cell Arteriopathy
NEJM 374:1265-1275, Case 10-2016, 2016

Bone Marrow Necrosis and Fat Embolism Syndrome in Sickle Cell Disease: Increased Susceptibility of Patients with Non-SS genotypes and a Possible Association with Human Parvovirus B19 Infection
Blood Rev 28:23-30, Tsitsikas, D.A.,et al, 2014

Sickle Cell Trait & Transient Monocular Blindness, Case Study
Am J Ophthalmol 8l:850, Finelli,P.F., 1976

Complicated Migraine & Hemoglobin AS in Nigerians
BMJ 2:62l, Osuntokun,B.O.,et al, 1972

Sickle Cell Disease & Monocular Blindness in Africans
Lancet Letter p 222 Jul 27, Konotey-Ahulu,F., 1968

Sicklemia
Ann Int Med 42:1065, Ende,N.,et al, 1955

A Case of Acute Akinetic Mutism and Encephalopathy
Neurol 99:761-766, Jain, V.,et al, 2022

Fat Embolism Syndrome in Sickle Cell Disease
J Clin Med 9:1-12, Tsitsikas, D.A.,et al, 2020

Cerebral Fat Embolism Syndrome in Sickle Cell Anaemia/�-Thalassemia: Importance of Susceptibility-weighted MRI
Clin Radiol 67:1023-1026, Mossa-Basha, M.,et al, 2012

An Unconsious Girl with Sickle-Cell Disease
Lancet 361:136, van Mierlo,T.D.,et al, 2003

Stroke Prevention and Treatment in Sickle Cell Disease
Arch Neurol 58:565-568, Adams,R.J., 2001

The Spectrum of Brain MR Abnormalities in Sickle-Cell Disease:A Report from the Cooperative Study of Sickle Cell Disease
AJNR 17:965-972, Moser,F.G.,et al, 1996

Risk of Recurrent Stroke in Patients with Sickle Cell Disease Treated with Erythrocyte Transfusions
J Pediatr 126:896-899, Pegelow,C.H.,et al, 1995

Stroke in a Cohort of Patients with Homozygous Sickle Cell Disease
J Pediatr 120:360-366, Balkaran,B.,et al, 1992

Cerebral Thrombosis in B-Thalassemia/Hemoglobin E Disease
Stroke 21:812-816, Wong,V.,et al, 1990

Hematologic Disorders and Ischemic Stroke
Stroke 21:1111-1121, Hart,R.G.&Kanter,M.C., 1990

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

Neurologic Complications of Hemoglobin SC Disease
Arch Neurol 41:289-292, Fablan,R.H.,et al, 1984

Spinal Cord Infarction in a Patient with Sickle Cell Anemia
Neurol 30:1072-1076, Rothman,S.M.,et al, 1980

The Natural History of Stroke in Sickle Cell Disease
Am J Med 65:461-471, Powars,D.,et al, 1978

Spinal Cord Compression in Thalassaemia
JNNP 40:1120 1977., Cross,J.N.,et al, 1977

A Comparison of the Physical & Intellectual Development of Black Children with & without Sickle-Cell Trait
Pediatrics 56:1021, McCormack,M.K.,et al, 1975

Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Sickle Cell Anemia
J Neurosurg 43:483, Ammoumi,A.A.,et al, 1975

Perceptual-Motor Dysfunction in Children w/Sickle Cell Trait
Perceptual & Motor Skills 36:234973., Flick,G.L.,et al, 1973

Occlusion of Large Cerebral Vessels in Sickle-Cell Anemia
NEJM 287:845, Stockman,J.A.,et al, 1972

Spinal Cord Infarction Associatred with The Sickle Cell Trait
Paraplegia 7:282, Wolman,L.,et al, 1970



Showing articles 0 to 29 of 29