Demography, Asia, West, Saudi Arabia

Transcription

1 Demography, Asia, West, Saudi Arabia Abdulkareem, A., Al-Abdulkareem, F. F. C. M., Seifeddin, G. and Ballal, M. D. (1998). Consanguineous marriage in an urban area of Saudi Arabia: Rates and adverse health effects on the offspring. Journal of Community Health 23: Al Aqeel, A., Ozand, P. T., Brismar, J., Gascon, G. G., Brismar, G., Nester, M. and Sakati, N. (1992). Saudi variant of multiple sulfatase deficiency. Journal of Child Neurology 7: S12 - S21. Al Aqeel, A. A., Ozand, P. T., Gascon, G. G., Hughes, H., Reynolds, C. T. and Subramanyam, S. B. (1992). Response of 6-pyruvoyl-tetrahydropterin synthase deficiency to tetrahydrobiopterin. Journal of Child Neurology 7: S26 -S30. Al Hussain, M. and Al Bunyan, M. (1997). Consanguineous marriages in a Saudi population and the effect of inbreeding on prenatal and postnatal mortality. Annals of Tropical Paediatrics 17: al-eissa, Y. and Ba'Aqeel, H. S. (1991). Low birthweight in Riyadh, Saudi Arabia: incidence and risk factors. Annals of Tropical Paediatrics 11: al-eissa, Y. A. (1995). Febrile seizures: Rate and risk factors of recurrence. Journal of Child Neurology 10: al-eissa, Y. A., Ba'Aqeel, H. S., Haque, K. N., Abo Bakr, A. M., al-kharfy, T. M., Khashoggi, T. Y. and al-husain, M. A. (1995). Determinants of term intrauterine growth retardation: the Saudi experience. American Journal of Perinatology 12: Algwiser, A. A. and Fachartz (1990). Premarital mortality at the Armed Forces Hospital Riyadh, Saudi Arabia: five year review of 22,203 births. Annals of Saudi Medicine 10: Al-Mazrou, Y. Y., Farid, S. M. and Khan, M. U. (1995). Changing marriage age and consanguineous marriage in Saudi females. Annals of Saudi Medicine 15: Al-Meshari, A., Niazi, M., Hawass, N., El-Badawi, M., Fatani, J. A. G. and Edress, Y. (1990). Cytogenetic investigation on fetuses from spontaneous abortions. Saudi Medical Journal 11: Al-Nadji, K. N., Al-R'shaid, W. A., Al-Atecqi, W. A. and Mahmeed, M. A. (1989). Pattern of morbidity among hospitalised children - a one-year retrospective study. Journal of the Kuwait Medical Association 23: Bahakim, H. M., Bangboye, E. A., Mahdi, A. H., Al-Mugeiren, M. M. and Familusi, J. B. (1993). Pediatric inpatients at the King Khalid University Hospital, Pujadh, Saudi Arabia, Annals of Saudi Medicine 13: 8-13.

2 Brismar, J. (1992). CT and MRI of the brain in inherited neurometabolic disorders. Journal of Child Neurology 7: S112 - S131. Cook, J. D., Gascon, G. G., Haider, A., Coates, R., Shigsby, B., Ozand, P. T. and Banna, M. (1992). Congenital muscular dystrophy with abnormal radiographic myelin pattern. Journal of Child Neurology 7: S51-S63. El-Hag, El-Awad, M. and Sivasankaran, S. (1992). Neural tube defects in the South West region of Saudi Arabia. Annals of Saudi Medicine 12: el-hazmi, M. A., al-swailem, A. R., Warsy, A. S., al-swailem, A. M., Sulaimani, R. and al-meshari, A. A. (1995). Consanguinity among the Saudi Arabian population. Journal of Medical Genetics 32: El-Hazmi, M. A. F. (1982). Haemoglobin disorders: a pattern for thalassaemia and haemoglobinaopathies in Arabia. Acta Haematologica 68: El-Hazmi, M. A. F., Al-Swailem, A. R., Al-Faleh, F. Z. and Warsy, A. S. (1986). Frequency of glucose-6-phosphate dehydrogenase, pyruvate kinase and hexokinase deficiency in the Saudi population. Human Heredity 36: El-Hazmi, M. A. F., Jabbar, F. A., Al-Faleh, F. Z., Al-Swailem, A. R. and Warsy, A. S. (1991). Patterns of sickle cell, thalassaemia and glucose-6-phosphate dehydrogenase deficiency genes in north-western Saudi Arabia. Human Heredity 41: El-Hazmi, M. A. F. and Warsy, A. S. (1986). Glucose-6-phosphate dehydrogenase polymorphism in the Saudi population. Human Heredity 36: El-Hazmi, M. A. F. and Warsy, A. S. (1989). Frequency of glucose-6-phosphate dehydrogenase phenotypes and deficiency in Al-Baha. Human Heredity 39: Gascon, G. G., Ozand, P. T. and Erwin, R. E. (1992). GMI gangliosidosis type 2 in two siblings. Journal of Child Neurology 7: S41-S50. Gascon, G. G., Youssef, N. G., Subramanyam, S. B. and Ozand, P. T. (1992). Coincident neuraminidase and aspatocyclase deficiency associated with chromosome 9q paracentric inversion in a Saudi family. Journal of Child Neurology 7: S73-S78. Hannan, M. A., Waghray, M., Sigut, D. and Ozand, P. T. (1992). Increased radiosensitivity of cell lines derived from a Down's syndrome patient with ocular telangiectasia. Journal of Child Neurology 7: S83-S87. Haque, K. N. and Bashi, O. (1988). Premarital mortality at King Khalid University Hospital, Riyadh. Annals of Saudi Medicine 8:

3 Kalloghlian, A., Gleipach, H. and Ozand, P. T. (1992). A patient with propionic academia managed with continuous insulin and total parental nutrition. Journal of Child Neurology 7: S88-S91. Mahdi, A. H. (1991). Genetically determined neurodegenerative disorders: experiences in Saudi Arabia. Annals of Tropical Paediatrics 11: Mesleh, R. (1985). Prenatal mortality at the Pujadh Armed Forces Hospital, Pujadh. Saudi Medical Journal 6: Millat, W. A. and Florey, C. D. (1992). Perinatal mortality in Jeddah, Saudi Arabia. International Journal of Epidemiology 21: Mir, N. A., Galczek, W. C. and Soni, A. (1992). Easily identifiable congenital malformations in children; survey of incidence and patterns in 32,332 liveborn neonates. Annals of Saudi Medicine 12: Nester, M. J., Sakati, N. and Greer, W. (1992). Unknown dystrophic syndrome and developmental delay in Saudi Arabia. Journal of Child Neurology 7: S64-S68. Ozand, P. T., Devol, E. B. and Gascon, G. G. (1992). Neurometabolic diseases at a national referral center: five years experience at the King Faisal Specialist Hospital and Research Centre. Journal of Child Neurology 7: S4-S11. Ozand, P. T. and Gascon, G. G. (1992). Heterogeneity of carboxypeptidtase activity in infantile- onset galactosialidosis. Journal of Child Neurology 7: S31-S40. Ozand, P. T. and Gascon, G. G. (1992). Treatment of inherited neurometabolic diseases: the future. Journal of Child Neurology 7: S132-S140. Ozand, P. T., Waghray, M., Cook, J. D., Sheth, K. and Gaseon, G. G. (1992). Riyadh chromosome breakage syndrome: mental retardation with depigmentation of the skin and hair. Journal of Child Neurology 7: S79-S82. Panter-Brick, C. (1991). Parental responses to consanguinity and genetic disease in Saudi Arabia. Social Science and Medicine 33: Panter-Brick, C. (1992). Coping with an affected birth: genetic counselling in Saudi Arabia. Journal of Child Neurology 7: S69- S72. Saedi-Wong, S., Al-Frayh, A. and Wong, H. Y. H. (1989). Socio-economic epidemiology of consanguineous matings in the Saudi Arabian population. Journal of Asian and African Studies 24: Saedi-Wong, S. and Al-Frayh, A. R. (1989). Effects of consanguineous matings on anthropometric measurements of Saudi newborn infants. Family Practice 6:

4 Salih, M. A., Mahdi, A. H., al-jarallah, A. A., al-jarallah, A. S., al-saadi, M., Hafeez, M. A. and Aziz, S. A. (1996). Childhood neuromuscular disorders: a decade's experience in Saudi Arabia. Annals of Tropical Paediatrics 16: Samuel, A. P. W., Saha, N., Acquaye, J. K., Omer, A., Ganeshaguru, K. and Hassounh, E. (1986). Association of red cell glucose-6-phosphate dehydrogenase with haemoglobinopathies. Human Heredity 36: Serenius, F. (1988). Attained growth of privileged Saudi children during the first three years of life. Acta Paediatrica Scand 346: Serenius, F., Edresse, A. W. and Swailem, A. R. (1988). Characteristics of the obstetric population in a Saudi maternity hospital. Acta Paediatrica Scand 346: Serenius, F., Fougerouse, D. and Sebai, Z. (1988). Growth and nutritional status of rural preschool children in Saudi Arabia. Acta Paediatria Scand 346: Serenius, F. and Hofvander, Y. (1988). The ecological context of child health in Saudi Arabia. Acta Paediatrica Scand 346: Serenius, F. and Swailem, A. R. (1988). Growth and nutritional status of less privileged urban children in Saudi Arabia. Acta PaediatricsaScand 346: Serenius, F., Swailem, A. R. and Edresse, A. W. (1988). Size at birth of infants in a Saudi maternity hospital. Acta Paediatrica Scand 346: Serenius, F., Swailem, A. R., Edresse, A. W. and Hofvander, Y. (1988). Patterns of breast feeding and weaning in Saudi Arabia. Acta Paediatrica Scand 346: Serenius, F., Swailem, A. R., Edresse, A. W. and Ohlsson, A. (1988). Causes of prenatal death at a Saudi maternity hospital. Acta Paediatrica Scand 346: Simin, S. W., Al-Frayh, A. R. and Wong, H. Y. H. (1989). Socioeconomic epidemiology of consanguineous matings in the Saudi Arabian population. Journal of Asian and African Studies 24: Subramanyam, S. B., Tipirneni, A., Youssef, N., Gascon, G. G. and Ozand, P. T. (1992). Biochemical heterogeneity of infantile central nervous system spongy degeneration. Journal of Child Neurology 7: S22-S25. Swailem, A. R., Serenius, F., Edresse, A. W. and Ohlsson, A. (1988). Prenatal mortality in a Saudi maternity hospital. Acta Paediatrica Scand 346: Thalji, A. A., Abu Osba, Y. K., Hann, R. W., Shamma'a, J. and Handan, J. (1986). Incidence of neural tube defects in the eastern province of Saudi Arabia. Journal of the Kuwait Medical Association 20:

5 Thomas, E. (1992). Dietary management of inborn errors of amino acid metabolism with protein-modified diets. Journal of Child Neurology 7: S92-S111. Zakzouk, S. M., Sobki, S. H., Mansour, F. and Al-Anazy, F. H. (1995). Hearing impairment in association with distal renal tubular acidosis among Saudi children. Journal of Laryngology and Otology 109: