Methods A self-administered questionnaire was mailed to 600 randomly selected pediatricians,
family practice physicians, emergency medicine physicians and general practitioners, …

Mutations in three different genes of phosphorylase kinase (Phk) subunits, PHKA2, PHKB
and PHKG2, can give rise to glycogen storage disease of the liver. The autosomal-recessive, …

Rihani R, Barbar M, Faqih N, Halalsheh H, Hussein A, Al‐Zaben AH, Rahman FA, Sarhan M.
Unrelated cord blood transplantation can restore hematologic and immunologic functions …

Causes of recurrent bowel intussusception in infancy are rarely identified and uncommon
causes such as gluten sensitive enteropathy are not well recognized. We report a 3 year-old …

We have correlated flow abnormalities in the hepatic vasculature with histological findings
in the liver to determine the accuracy of Doppler ultrasound in the diagnosis of liver cirrhosis …

In patients with Wilson disease (WD), an autosomal recessive disorder, toxic accumulation
of copper results in fatal liver disease and irreversible neuronal degeneration. ATP7B, the …

We review the past, present and future state of mental health care in the Kingdom of Saudi
Arabia (KSA). The past is reviewed prior to the modern era, discussing early explanations and …

There are a few reports about the size of the problem of vesicoureteral reflux (VUR) in
developing countries. We attempted in our study to assess the experience of this problem in …

Results Twenty-four children presented with clinical data fulfilling the criteria. They represent
zero to one case of 30 to 50 admissions per day during the period of the study with …

Polyarteritis nodosa (PAN) is a rare type of childhood vasculitis. We report the case of a 10-year-old
boy who was referred to our hospital following an appendicectomy with fever, …