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Dive into the research topics where J. Chawluk is active.

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Featured researches published by J. Chawluk.


Cancer | 1988

Positron emission tomography in patients with glioma. A predictor of prognosis.

Jane B. Alavi; Abass Alavi; J. Chawluk; Michael Kushner; John Powe; William F. Hickey; Martin Reivich

Positron emission tomography (PET) studies have been performed using 18‐F‐fluorodeoxyglucose in 29 adult subjects with primary brain tumors. Seventy‐two percent of the patients were treated previously. The glucose metabolic state in the lesions was increased in 16 patients, and was normal or decreased in 13 patients. The hypermetabolic tumors tended to behave in a more malignant fashion. Patients with hypermetabolic tumors had a median survival of 7 months after PET scan, compared to 33 months for those with hypometabolic lesions. Among the high‐grade glioma patients, the PET results separated them into a good prognosis group (hypometabolic, with 78% 1‐year survival) and a poor prognosis group (hypermetabolic, with a 29% 1‐year survival after PET). These results suggest that glucose metabolic studies may provide an independent measure of the aggressiveness of a brain tumor, and may supplement pathologic grading.


Ophthalmology | 1989

Alzheimer's Disease with Prominent Visual Symptoms: Clinical and Metabolic Evaluation

Motohiro Kiyosawa; Thomas M. Bosley; J. Chawluk; Dara G. Jamieson; Norman J. Schatz; Peter J. Savino; Robert C. Sergott; Martin Reivich; Abass Alavi

The authors examined eight patients with dementia of the Alzheimers type (DAT), five with prominent visual symptoms early in the illness (VS) and three with no visual symptoms (NVS). Results of neuro-ophthalmologic examinations on VS patients showed relatively consistent abnormalities in figure copying, color vision tested by isochromatic plates, and stereopsis. Cerebral glucose metabolism determined by 18F-fluoro-2-deoxyglucose positron emission tomography (PET) was unchanged in primary visual cortex of VS and NVS patients compared with 12 normal volunteers of similar age and sex. Glucose metabolism in VS patients was decreased by 45 and 34% in left and right visual association cortex (P less than 0.01 and P less than 0.05, respectively) and 34 and 37% in left and right inferior parietal cortex (P less than 0.05) compared with controls; NVS patients had no significant metabolic alteration in these areas. Symptoms, physical examination, and metabolic imaging imply that these patients are a heterogenous but distinct clinical subgroup of DAT often with mild dementia who have visual symptoms due primarily to visual agnosia.


Seminars in Nuclear Medicine | 1986

Positron emission tomography imaging of regional cerebral glucose metabolism

Abass Alavi; Robert Dann; J. Chawluk; Jane B. Alavi; Michael Kushner; Martin Reivich

The (F-18) fluorodeoxyglucose (FDG) technique to measure local cerebral metabolic rate for glucose (LCMRglu) is well accepted and widely used by many institutions around the world. A large number of studies has been carried out in normal volunteers and patients with a variety of CNS disorders. Several investigators have noted that no significant age-related changes in cerebral glucose use occur with normal aging. Some important and interesting findings have been revealed following sensory, motor, visual, and auditory stimulations. Functional imaging with FDG in certain neurologic disorders has dramatically improved our understanding of their underlying pathophysiologic phenomena. Some abnormalities detected on the positron emission tomography (PET) images have no corresponding changes on either x-ray computed tomograms (XCT) or magnetic resonance images (MRI). In patients with Alzheimers disease, primary sensorimotor, visual, and cerebellar metabolic activity appears relatively preserved. In contrast, parietal, temporal, and to some degree, frontal glucose metabolism is significantly diminished even in the early stages of the disease. Patients with Huntingtons disease and those at risk of developing this disorder have a typical pattern of diminished CMRglu in the caudate nuclei and putamen. In patients with stroke, PET images with FDG have demonstrated abnormal findings earlier than either XCT or MRI and with a wider topographic distribution. FDG scans have revealed interictal zones of decreased LCMRglu in approximately 70% of patients with partial epilepsy. The location of the area of hypometabolism corresponds to the site of the epileptic focus as determined by electroencephalography and microscopic examination of the resected tissue. Ictal scans during partial seizures demonstrate areas of hypermetabolism corresponding to the sites of seizure onset and spread. Several investigators have reported relative hypofrontal CMRglu in patients with schizophrenia. In our center, FDG scans from patients with schizophrenia were successfully differentiated from those obtained in normal controls. Finally, our preliminary data (using PET, XCT, and MRI) in patients with CNS disorders indicate that MRI provides excellent delineation of the structural abnormalities. It may prove to be superior to XCT in the evaluation of certain diseases such as cerebral ischemia and infarcts, head injury, tumors, and white matter lesions. Metabolic imaging with FDG provides functional information not obtainable with either MRI or NMR spectroscopy. Therefore, PET studies will play a complementary role to the anatomic imaging in the management of patients with CNS disorders.


Neurology | 1987

Metabolic and clinical correlates of acute ischemic infarction.

Michael Kushner; Martin Reivich; C. Fieschi; F. Silver; J. Chawluk; M. Rosen; Joel H. Greenberg; Allan M. Burke; Abass Alavi

We studied cerebral metabolism, anatomy, and clinical status in 36 patients with acute cerebral ischemia. Results from FDG-PET were compared with CT to find the relationships between the metabolic, anatomic, and clinical findings. Metabolic abnormalities seen on PET frequently were more extensive than the corresponding CT findings. The pattern of metabolic abnormality was significantly related to both the type of clinical syndrome and the degree of eventual recovery. No such relationships were found for the CT results. We conclude that studies of cerebral metabolism are of value in establishing prognosis after acute cerebral ischemia. Also, knowledge of the patterns of cerebral dysmetabolism provides a powerful means for the localization of clinical function.


Neurology | 1988

Atherosclerotic carotid artery disease in patients with retinal ischemic syndromes

J. Chawluk; Michael Kushner; William J. Bank; F. Silver; Dara G. Jamieson; Thomas M. Bosley; D. J. Conway; D. Cohen; Peter J. Savino

The extracranial carotid systems of 105 patients with retinal ischemia were examined using B-mode ultrasonography with integrated pulsed Doppler. Sixty-four patients had amaurosis fugax (AF), 17 central retinal artery occlusions (CRAO), and 21 branch retinal artery occlusions (BRAO). The prevalence of carotid stenosis (≥60%) ipsilateral to the symptomatic eye was low (16%). Eighty-six percent of AF patients had either no plaque or plaque causing less than a 60% stenosis. A significant proportion of subjects with normal duplex scans had alternative explanations for their retinal ischemia (eg, migraine, cardiac embolus). Patients with Hollenhorst plaques were more likely to have stenotic or ulcerated plaque (p = 0.04). The degree of carotid stenosis correlated significantly with the number of vascular risk factors identified in individual patients (p = 0.02). The presence of risk factors was more common in CRAO and BRAO patients compared with the AF group. Combined ultrasound-Doppler investigations of the carotid bifurcation are valuable noninvasive tools for the screening of patients with retinal ischemia.


Neurology | 1990

Cerebral blood flow variations in CNS lupus

Michael Kushner; M. Tobin; Franz Fazekas; J. Chawluk; Dara G. Jamieson; B. Freundlich; S. Grenell; L. Freemen; Martin Reivich

We studied the patterns of cerebral blood flow (CBF), over time, in patients with systemic lupus erythematosus and varying neurologic manifestations including headache, stroke, psychosis, and encephalopathy. For 20 paired xenon-133 CBF measurements, CBF was normal during CNS remissions, regardless of the symptoms. CBF was significantly depressed during CNS exacerbations. The magnitude of change in CBF varied with the neurologic syndrome. CBF was least affected in patients with nonspecific symptoms such as headache or malaise, whereas patients with encephalopathy or psychosis exhibited the greatest reductions in CBF. In 1 patient with affective psychosis, without clinical or CT evidence of cerebral ischemia, serial SPECT studies showed resolution of multifocal cerebral perfusion defects which paralleled clinical recovery.


Neurology | 1987

Cerebral blood flow in systemic lupus erythematosus with or without cerebral complications

Michael Kushner; J. Chawluk; F. Fazekas; B. Mandell; Allan M. Burke; Jurg L. Jaggi; M. Rosen; Martin Reivich

We measured mean cerebral blood flow (CBF) in 25 lupus patients using the xenon-133 method. The CBF was normal in lupus patients without cerebral disease and also in CNS lupus patients in remission. The CBF was lower than normal during bouts of cerebral lupus (p < 0.001). Repeat studies showed a stereotyped pattern consisting of depressed CBF during exacerbation of CNS disease and normalization of CBF during remission (p < 0.01). These results show that CBF is a sensitive indicator of activity of CNS disease and that the direction of change in CBF reflects the clinical course of CNS lupus.


Neurology | 1988

Resolving metabolic abnormalities in a case of pure alexia

F. Silver; J. Chawluk; Thomas M. Bosley; M. Rosen; Robert Dann; R. C. Sergott; Abass Alavi; Martin Reivich

We report resolving metabolic abnormalities corresponding to clinical improvement in a patient with pure alexia secondary to acute cerebral infarction. Local cerebral glucose metabolism (lCMRgl) was measured with positron emission tomography (PET) using 18F-fluorodeoxyglucose (18F-FDG) close to ictus and 41/2 months later. Serial CTs and a subsequent MRI demonstrated small, unchanging left-hemispheric lesions involving the area of the lateral geniculate body and the splenium of the corpus callosum. PET demonstrated the evolution of the metabolic abnormality resulting from intrahemispheric (lateral geniculate) and interhemispheric (splenium) disconnection in the absence of occipital lobe infarction. This case illustrates that cerebral disconnection can result in the syndrome of pure alexia. The factors accounting for focal hypometabolism in the absence of cerebral infarction are discussed.


Neurology | 1988

Positron emission tomography in a patient with progressive multifocal leukoencephalopathy

Motohiro Kiyosawa; Thomas M. Bosley; Abass Alavi; N. Gupta; C. H. Rhodes; J. Chawluk; Michael Kushner; Peter J. Savino; Robert C. Sergott; Norman J. Schatz; Martin Reivich

A 56-year-old man with chronic lymphocytic leukemia, progressive multifocal leukoencephalopathy, and a dense left homonymous hemianopia had 18F-fluorodeoxyglucose positron emission tomography. Cortical glucose metabolism was decreased in the right cerebral hemisphere and the left cerebellar hemisphere. To our knowledge, this is the first demonstration of cerebral and cerebellar hypometabolism due solely to white matter disease.


Gerontology | 1987

Local Cerebral Metabolic Changes in Acute Ischemic Strokes

Michael Kushner; C. Fieschi; Abass Alavi; F. Silver; J. Chawluk; Martin Reivich

Positron emission tomography (PET) studies with 18F deoxyglucose were completed in 35 patients with acute ischemic strokes. Twelve cases were studied within 72 h, 23 between 4 and 14 days. Results indicate the functional and prognostic significance of early tomography studies of metabolism, and anticipate possible use of metabolic imaging in the evaluation of treatment.

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Martin Reivich

University of Pennsylvania

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Abass Alavi

Hospital of the University of Pennsylvania

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Michael Kushner

University of Pennsylvania

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Robert Dann

University of Pennsylvania

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Dara G. Jamieson

University of Pennsylvania

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M. Rosen

University of Pennsylvania

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F. Silver

University of Pennsylvania

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Howard I. Hurtig

University of Pennsylvania

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Jane B. Alavi

University of Pennsylvania

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