El Rifai Nahida

Summary

Country: France

Publications

  1. ncbi request reprint Neuronal intranuclear inclusion disease presenting as chronic intestinal pseudo-obstruction in the neonatal period in the absence of neurologic symptoms
    Nahida El-Rifai
    Department of Pediatrics and Pediatric Gastroenterology, Makassed General Hospital, Beirut, Lebanon
    J Pediatr Gastroenterol Nutr 42:321-3. 2006
  2. ncbi request reprint Gastropathy and gastritis in children with portal hypertension
    Nahida El-Rifai
    Department of Pediatric Gastroenterology, Jeanne de Flandre Hospital, France
    J Pediatr Gastroenterol Nutr 45:137-40. 2007
  3. doi request reprint Pseudo-Bartter's syndrome revealing cystic fibrosis in an infant caused by 3849 + 1G>A and 4382delA compound heterozygosity
    El Rifai Nahida
    Department of Pediatrics, Makassed General Hospital, Beirut, Lebanon
    Acta Paediatr 100:e234-5. 2011

Collaborators

  • Frederic Gottrand
  • Nahida El-Rifai
  • Dominique Guimber
  • Francoise Boman
  • Karine Mention
  • Laurent Michaud
  • Dominique Turck
  • Francis Jaubert
  • Khalil Tayyarah
  • Abir Baydoun
  • Nabil Daoud

Detail Information

Publications3

  1. ncbi request reprint Neuronal intranuclear inclusion disease presenting as chronic intestinal pseudo-obstruction in the neonatal period in the absence of neurologic symptoms
    Nahida El-Rifai
    Department of Pediatrics and Pediatric Gastroenterology, Makassed General Hospital, Beirut, Lebanon
    J Pediatr Gastroenterol Nutr 42:321-3. 2006
  2. ncbi request reprint Gastropathy and gastritis in children with portal hypertension
    Nahida El-Rifai
    Department of Pediatric Gastroenterology, Jeanne de Flandre Hospital, France
    J Pediatr Gastroenterol Nutr 45:137-40. 2007
    ..PHG is frequently found in children with portal hypertension, and it develops regardless of the cause of the portal hypertension...
  3. doi request reprint Pseudo-Bartter's syndrome revealing cystic fibrosis in an infant caused by 3849 + 1G>A and 4382delA compound heterozygosity
    El Rifai Nahida
    Department of Pediatrics, Makassed General Hospital, Beirut, Lebanon
    Acta Paediatr 100:e234-5. 2011
    ..It explains the lung involvement with the dehydration and electrolyte disturbances. The role of the mutation in exon 24 in cases of CF with PB syndrome remains to be determined...