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Your search keyword '"Berkel, Izzet"' showing total 17 results
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17 results on '"Berkel, Izzet"'

4. Localization of an ataxia-telangiectasia gene to chromosome 11q22-23

Author

Gatti, Richard A., Berkel, Izzet, Boder, Elena, Braedt, Gary, Charmley, Patrick, Concannon, Patrick, Ersoy, Fugen, Foroud, Tatiana, Jaspers, Nicholas G.J., Lange, Kenneth, Lathrop, G. Mark, Leppert, Mark, Nakamura, Yasuke, O'Connell, Peter, Paterson, Malcolm, Salser, Winston, Sanal, Ozden, Silver, Jack, Sparkes, Robert S., Susi, Ellen, Weeks, Daniel E., Wei, Shan, White, Ray, and Yoder, Freda

Subjects
Genetic disorders -- Research, Ataxia telangiectasia -- Genetic aspects, Environmental issues, Science and technology, Zoology and wildlife conservation
Published
1988

8. Griscelli syndrome: Report of Three Cases

Author

Göğüş, Safiye, primary, Topçu, Meral, additional, Küçükali, Türkan, additional, Akçören, Zuhal, additional, Berkel, Izzet, additional, Ersoy, Figen, additional, Günay, Meral, additional, and Saatçi, Işil, additional

Published
1995
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12. Geophagia Associated with Iron-deficiency Anemia, Hepatosplenomegaly, Hypogonadism and Dwarfism.

Author

Say, Burhan, Özsoylu, Sinasi, and Berkel, Izzet

Subjects
IRON deficiency anemia, HYPOGONADISM, SEXUAL dysfunction, DWARFISM, LIVER diseases, PATIENTS
Abstract

The article presents the results of clinical and laboratory studies on 29 children with geophagia, serious growth retardation, and delayed sexual maturation. Other findings in these children included iron deficiency anemia, mild to moderate liver changes and nonspecific intestinal mucosal changes. Many complications such as lead poisoning and intestinal parasitosis may follow the ingestion of unusual substances for food. Iron deficiency is seen frequently in such patients, although some investigators believe that the pica is the result of pre-existing iron deficiency rather that its cause.

Published
1969
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13. Griscelli syndrome: Report of Three Cases

Author

Göğüs, Safiye, Topçu, Meral, Küçükali, Türkan, Akçören, Zuhal, Berkel, Izzet, Ersoy, Figen, Günay, Meral, and Saatçi, Isil

Abstract

The clinical features of three children with Griscelli syndrome and autopsy findings of two are presented. The patients were 5 years, 9 months, and 3 months old, respectively. Clinical features included partial albinism, hepatosplenomegaly, and various neurological symptoms. Light and electron microscopic studies of the skin were compatible with Griscelli syndrome. Postmortem examination of the viscera and central nervous system revealed lymphohistiocytic infiltration with erythrophagocytosis. Bilateral diffuse involvement of the central nervous system, cranial nerve, and spinal cord was detected in both cases.

Published
1995
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15. Goodpasture's Syndrome (Pulmonary Hemosiderosis with Nephritis).

Author

Ozsoylu, Sinasi, Hicsonmez, Gonul, Berkel, Izzet, Say, Burhan, and Tinaztepe, Behcet

Subjects
HEMOSIDEROSIS, INTERSTITIAL nephritis, BOYS, CLINICAL indications, PEDIATRIC respiratory diseases, RESPIRATORY infections in children, PEDIATRIC nephrology
Abstract

Presents the clinical case of a six-year-old boy with Goodpasture's Syndrome or pulmonary hemosiderosis with nephritis. Complaints of pallor, respiratory distress, and palpitation; Fever for a short time in the past three months; Onset of sudden coughing 10 weeks later; Blood pressure; Respiratory wheezing and rhonchi in both lung fields; Bilateral papiledema.

Published
1976
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