This book describes a study aiming to update Iraqi pediatricians' research productivity in the field of nephrology using bibliometric methods, and analysis of the contribution of Iraqi pediatrician...
This book describes a study aiming to update Iraqi pediatricians' research productivity in the field of nephrology using bibliometric methods, and analysis of the contribution of Iraqi pediatrician...
Broccoli (Brassica oleracea var. italica) is one of the most economically important vegetable crops. It belongs to world primary vegetables and its production quantity. Broccoli belongs to the Bras...
Hereditary spherocytosis is an abnormality of red blood cells, or erythrocytes. The disorder is caused by mutations in genes relating to membrane proteins that allow for the erythrocytes to change ...
Iron is the necessary molecule for cellular metabolism and is an imperative nonorganic substance, that plays a major role inoxygentransport, short-term oxygen storage., electron transfer, DNA synth...
Vitamin D is a group of fat-soluble secosteroids responsible for increasing intestinal absorption of calcium, magnesium, and phosphate, and multiple other biological effects. The major natural sour...
The New Iraqi Journal of Medicine was founded in 2005 and it became the official journal of the Iraqi Ministry of Health and Iraq headquarter of Copernicus Scientists International Panel. The journ...
Gilles de la Tourette syndrome is a neuro-psychiatric disorder that generally affects children with normal intelligence and can affect also talented children. Gilles de la Tourette syndrome was fir...
Epilepsy is a group of neurological disorders characterized by recurrent epileptic seizures. Epileptic seizures are episodes that can vary from brief and nearly undetectable periods to long periods...
Mental retardation has been recently called by the American Psychiatric Association" intellectual disability" despite that World Health Organization is still using the term "Mental retardation" in ...
Hypoparathyroidism is a rare endocrine disorder that can be congenital or acquired. The congenital disorder can result from aplasia or hypoplasia of parathyroids or occurs as a part of genetic synd...
The aim of this book is to review the available scientific evidence with aim of finding keys to overcome the therapeutic challenge associated with the emerging coronavirus global pandemic in 2020. ...
Hemifacial microsomia is a rare congenital, heterogeneous malformation disorder affecting predominantly unilateral face. The disorder is associated with unusual strange distortion of the face with ...
Non-syndromic agenesis of the corpus callosum is a rare congenital disorder that has not been described or documented in Iraq. In this book, two Iraqi infants with non-syndromic agenesis of the cor...
Prader-Willi syndrome (PWS) is a genetic disorder due to loss of function of specific genes. In newborns, symptoms include weak muscles, poor feeding, and slow development. Beginning in childhood, ...
Pervasive developmental disorder was first recognized by Grunya Efimovna Sukhareva in 1925. She called it autistic psychopathy. In 1938, Hans Asperger provided more detailed descriptions of childre...
Researchgate is an increasingly popular academic web site that has been increasingly used in the ranking of individual academics (physicians, scientists, researchers), and academic institutions. Sc...
Coffin Siris syndrome is very rare genetic syndrome.THE TOTAL NUMBER OF THE REPORTED PATIENTS WITH COFFIN SIRIS SYNDROME IS 169. Coffin Siris syndrome has been reported only once in Iraq. The first...