Bøker av Aamir Al Mosawi

Für viele der behindernden genetischen Erkrankungen wie die pädiatrische juvenile spinale Muskelatrophie (Wohlfart-Kugelberg-Welander-Syndrom) gibt es keine zufriedenstellende Therapie. In diesem Buch wird eine neuartige Therapie für die pädiatrische juvenile spinale Muskelatrophie beschrieben, die zu einer offensichtlichen Verbesserung führte, über die bisher noch nie berichtet wurde. Zwei nicht verwandte irakische Jungen mit pädiatrischer juveniler spinaler Muskelatrophie wurden beobachtet, und der stärker betroffene Junge wurde mit einer neuartigen Therapie behandelt, die innerhalb von weniger als einem Monat zu einer deutlichen Besserung führte. Der weniger stark betroffene Junge erhielt keine Behandlung und zeigte auch nach einigen Monaten keine Besserung.

Não há terapia satisfatória para muitas das doenças genéticas incapacitantes, tais como a atrofia muscular pediátrica da coluna vertebral juvenil (síndrome de Wohlfart Kugelberg Welander). O objectivo deste livro é descrever uma nova terapia para a atrofia muscular espinal juvenil pediátrica, que resultou numa melhoria óbvia que nunca foi relatada antes. Foram observados dois rapazes iraquianos não relacionados com a atrofia muscular espinal juvenil pediátrica, e aquele que foi mais severamente afectado foi tratado com uma nova terapia que resultou numa melhoria óbvia em menos de um mês. O rapaz menos afectado não recebeu qualquer tratamento e não mostrou qualquer melhoria após alguns meses.

Il n'existe pas de traitement satisfaisant pour de nombreuses maladies génétiques invalidantes telles que l'amyotrophie spinale juvénile de l'enfant (syndrome de Wohlfart Kugelberg Welander). L'objectif de cet ouvrage est de décrire une nouvelle thérapie pour l'amyotrophie spinale juvénile pédiatrique qui a entraîné une amélioration évidente, jamais rapportée auparavant. Deux garçons irakiens non apparentés atteints d'amyotrophie spinale juvénile ont été observés, et celui qui était le plus gravement atteint a été traité avec une nouvelle thérapie qui a entraîné une amélioration évidente en moins d'un mois. Le garçon moins atteint n'a reçu aucun traitement et n'a montré aucune amélioration après quelques mois.

Non esiste una terapia soddisfacente per molte malattie genetiche invalidanti come l'atrofia muscolare spinale giovanile pediatrica (sindrome di Wohlfart Kugelberg Welander). Lo scopo di questo libro è di descrivere una nuova terapia per l'atrofia muscolare spinale giovanile pediatrica che ha portato a un evidente miglioramento, mai riportato prima. Sono stati osservati due ragazzi iracheni non imparentati con l'atrofia muscolare spinale giovanile pediatrica e quello più gravemente colpito è stato trattato con una nuova terapia che ha portato a un evidente miglioramento in meno di un mese. Il ragazzo meno colpito non ha ricevuto alcun trattamento e non ha mostrato alcun miglioramento dopo pochi mesi.

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 pediatricians to the field of pediatric nephrology literature. Papers published by Iraqi pediatricians¿ in the field of pediatric nephrology were retrieved from ¿Web of Science¿ and ¿PubMed¿ . The number and types of papers, and author¿s h-index (Hirsch index) were analyzed. Papers published by researchers other than pediatricians such urologic surgeons, and basic sciences researchers were not included in this study. The vast majority of papers, 49 (92.4 %) were published by Aamir Jalal Al-Mosawi. Only four our papers were published by authors other than Aamir Jalal Al-Mosawi, and was carefully examined and found to include unreliable, non-authentic and largely misleading information. The work of Aamir Jalal Al-Mosawi represented the authentic reliable source about childhood renal disorders in Iraq.

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 first described in a book entitled ¿Malleus Maleficarum¿ which means "Witch's hammer" in the late 15th century. The book described a priest whose abnormal involuntary repetitive behaviors were considered to be related to possession by the devil. In the medical literature, Jean Marc Gaspard Itard, a French doctor was the first to describe a patient with this syndrome in 1825. The rather bizarre manifestations of the syndrome including involuntary movements and utterances can make an intelligent child a victim of the condition, and adversely affects his schooling and results in social rejection and consequently isolation. Awareness of this condition by the community, educators, and also medical practitioners are necessary to avoid the loss of affected children who can have the potential to be a talented individual in the future. Gilles de la Tourette syndrome has not been described or documented before in Iraq. The aim of this book is to describe the first case of this syndrome in Iraq.

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 its ICD-10 publication. There is no known therapeutic approach that can advance the mental functions to move the patient with mental retardation from the uneducable to educable mental retardation. The aim of this book is to describe a novel therapeutic approach which was successful in advancing the mental functions in a patient with uneducable (Moderate to severe) idiopathic mental retardation and making the child perfectly educable. This book is not about what was called historically a heroic or miraculous medicine, but it is all about providing a preliminary scientific evidence, changing perspectives and opening new frontiers.

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 Iraqi patient with Coffin Siris syndrome (Al Mosawi AJ,2006) was also the first patient in the Arab. The main aim of this book is to describe the second case of this syndrome in Iraq which is also the case number 170 in the world. The book also describes the historic documentation of the syndrome in the literature.