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559 results on '"Nazer, Hisham"'

1. Parenteral Nutrition

Author

Miqdady, Mohamad, Abdelhadi, Ruba A., Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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2. Vitamin Deficiencies and Excess

Author

Suliman, Gaafar I., Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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3. Breast Feeding

Author

Shohieb, Salah, Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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4. Malnutrition in Infancy

Author

Moya, Manuel, Bozo, Mahmoud, Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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5. Formula Feeding

Author

Koleilat, Aziz, Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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6. The Porphyrias

Author

Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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7. Drug-Induced Liver Injury

Author

Nazer, Lama H., Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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8. Portal Hypertension and Esophageal Varices

Author

Guindi, Mohamed A. El, Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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9. Cirrhosis and Ascites

Author

Shammout, Jumana, Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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10. Protein-Losing Enteropathy

Author

Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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11. Wilson Disease

Author

Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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12. Short Bowel Syndrome

Author

Abdelhadi, Ruba A., Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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13. Congenital Hepatic Fibrosis

Author

Nazer, Dena, Nazer, Hisham M, Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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15. Gastrointestinal Bleeding

Author

Gilger, Mark A., Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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16. Celiac Disease

Author

Nazer, Hisham M., Rawashdeh, Mohamed, Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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17. Chronic Diarrhea

Author

Shammout, Jumana, Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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18. Congenital Chloride Diarrhea

Author

Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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19. Functional Gastrointestinal Disorders

Author

Banoub, Hany, Nazer, Hisham M., Chong, Sonny K. F., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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20. Gut Motility Problem

Author

Hammo, Abdel-Hai, Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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21. The Esophagus

Author

Gilger, Mark A., Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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22. Peptic Ulcer Disease

Author

El Guindi, Mohamed A., Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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23. The Stomach

Author

Shammout, Jumana, Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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25. Enteral Feeding

Author

Bozo, Mahmoud, Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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26. Budd–Chiari Syndrome

Author

Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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27. Infantile Hypertrophic Pyloric Stenosis

Author

Nazer, Dena, Nazer, Hisham M., Elzouki, Abdelaziz Y., editor, Harfi, Harb A., editor, Nazer, Hisham M., editor, Stapleton, F. Bruder, editor, Oh, William, editor, and Whitley, Richard J., editor

Published
2012
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28. Genetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and Kuwait

Author

Hoglund, Pia, Auranen, Mari, Socha, Jerzy, Popinska, Kataryna, Nazer, Hisham, Rajaram, Usha, Al Sanie, Abdullah, Al-Ghanim, Mohammed, Holmberg, Christer, De la Chappelle, Albert, and Kere, Juha

Subjects
Diarrhea -- Genetic aspects, Gene mutations -- Research, Biological sciences
Abstract

Eight new mutations were found in a study of congenital chloride diarrhea (CLD) among populations in Finland, Poland, Saudi Arabia and Kuwait, bringing the total of known CLD gene mutations to 19. Mutations affect the same locus in all cases studied. Evidence of a major founder effect was seen in the Arab patients.

Published
1998

35. Fanconi's syndrome with hepatorenal glycogenosis associated with phosphorylase b kinase deficiency

Author

Sanjad, Sami A., Kaddoura, Rokia E., Nazer, Hisham M., Akhtar, Mohammed, and Sakati, Nadia A.

Subjects
Kidney diseases -- Physiological aspects, Glycogenosis -- Complications, Protein kinases -- Health aspects, Renal manifestations of general diseases -- Physiological aspects, Family and marriage, Health
Abstract

* Objective. - To describe two patients with Fanconi's nephropathy secondary to glycogen storage disease and speculate on the possible etiology. Design. - Convenience sample. Setting. - Tertiary care, referral center. Patients. - Two related children referred for failure to thrive, rickets, and hepatomegaly. Intervention. - Dietary and therapeutic measures for rickets and renal tubular acidosis. Measurements and Results. - The main laboratory findings were fasting hypoglycemia and massive glucosuria, with evidence of multiple renal tubular dysfunction characteristic of the Fanconi syndrome. Liver and kidney biopsy specimens were consistent with glycogen storage disease. Enzymatic assay of liver homogenates revealed marked deficiency of phosphorylase b kinase in one patient and absent activity in the other. Conclusion. - Phosphorylase b kinase deficiency may be causally related to hepatorenal glycogenosis with the Fanconi syndrome. More patients with this syndrome need to be studied before a definitive causal role is implicated. (AJDC 1993;147:957-959), Glycogen storage disease (GSD) associated with Fanconi's syndrome may be caused by phosphorylase b kinase deficiency. GSD is a rare inborn metabolic disorder affecting carbohydrate metabolism. Fanconi's syndrome is characterized by dysfunction of the kidney tubules. Phosphorylase b kinase is a liver enzyme involved in the breakdown of glycogen. Two related infants were diagnosed GSD and Fanconi's syndrome. Their symptoms were failure to thrive, diminished muscle tone, enlarged liver and rickets. Laboratory tests revealed hypoglycemia and excretion of large amounts of glucose in the urine. Enzyme tests showed phosphorylase b kinase deficiency in one infant and no phosphorylase b kinase activity in the other.

Published
1993

36. LETTERS.

Author

SCHNEIDER, RODNEY, WAGNER, GRETCHEN, DORYLAND, SYLVIA H., WOOD, ROY L., DZENGELESKI, EVELYN K., RICHARDSON, ANNA E., GHELIBOLIAN, NORAIR, SANDLER, BENJAMIN P., MURRAY, ARTHUR, HOGLUND, GUNNAR, NAZER, HISHAM, DILEY, JOHN, KING, JAMES, ROBERTSON, ALLEN R., WILSON, S. M., EILAND, MICHAEL M., CREEKMORE, H. L., LAKHANI, H. H., PALELLA, NICK, and CAYO, FELIX

Subjects
UNAFFILIATED voters, DEMOCRATS (United States), REPUBLICANS
Published
1956

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