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Nigerian Journal of Surgery : Official Publication of the Nigerian Surgical Research Society|June 7, 2017
Prognostic Factors and Outcome of Management of Ischemic Priapism in Zaria, NigeriaMuhammed Ahmed, Benjamin Augustine, Messi Matthew, et al.
La Tunisie Medicale|August 23, 2001
[Mucopolysaccharidoses in children. Experience of a general pediatric service. 11 cases]M Chaabouni, M Ben Slimen, M Boudawara, et al.
Journal of Applied Microbiology|April 5, 2019
Phytopathogenic and antagonistic potentialities of fungi associated with pistachio bark beetle, Chaetoptelius vestitus (Coleoptera, Curculionidae), infesting pistachio (Pistacia vera) in TunisiaK Hadj Taieb, H Gharsallah, I Ksentini, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Four families with loss of function mutations of the thyrotropin receptorN de Roux, M Misrahi, R Brauner, et al.
European Journal of Endocrinology|January 29, 2011
Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative formsR Reynaud, F Albarel, A Saveanu, et al.
Cureus|August 11, 2022
Triple-Negative Sjogren's Syndrome and Recurrent Pneumothorax: An Uncommon Presentation of Autoimmune DiseaseZiryab Imad, Yassin A Abdalla, Salih B Hamza, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiencyS Vallette-Kasic, A Barlier, C Teinturier, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 26, 1998
Three-year data from a comparative study with recombinant human growth hormone in the treatment of short stature in young children with intrauterine growth retardationA Fjellestad-Paulsen, P Czernichow, R Brauner, et al.
Archives of Disease in Childhood|January 6, 1999
Long-term follow up of 69 patients treated for optic pathway tumours before the chemotherapy eraC Cappelli, J Grill, M Raquin, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndromeS Hadj-Rabia, R Salomon, A Pelet, et al.
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