Synnynnäiset sairaudet ja häiriöt

Osteogenesis imperfecta (OI), also known as brittle bone disease, is a genetic disease involving primarily the skeleton but affecting all organ systems. It is an extremely …

Bringing together the most up-to-date information on congenital Mullerian anomalies, this comprehensive text explores advances in understanding the embryological causes of these …

This book presents muscular dystrophy (MD) as a group of genetic diseases with a worldwide occurrence of about 1 in 3,500 births that causes muscle wasting and weakening. It …

Das neue Buch von Oliver Sacks entführt den Leser in die Welt der Südseeinseln. Die erste der Reisen führt uns zu zwei Inseln, wo ein überdurchschnittlich hoher Bevölkerungsanteil …

This is by far the most complete and comprehensive study ever written for parents of autistic children, and for teachers, child specialists, and other professionals who care for …

Tämän Liisa Mirjam Helimäen kuudennen kirjan aiheena on Turnerin oireyhtymä.Se tarkoittaa naiselle sikiövaiheen alussa tullutta kromosomipoikkeamaa sukusoluissa. Se aiheuttaa …

Neural tube defects are the second most common cause of perinatal death from birth defects in the United Kingdom. In this important book, leading scientists evaluate the latest …

Dana Creighton and her mother both were affected by the same inherited cerebellar degeneration, known as ataxia--a loss of control over body movements. Both were treated by a …

Dieses Buch analysiert die Rechtslage im Hinblick auf die heterologe Insemination in Deutschland, Österreich und der Schweiz. Den Schwerpunkt bildet dabei die Untersuchung des im …

Cosa si prova a non poter avere un figlio? Quanto è difficile comunicare alla coppia una diagnosi di sterilità? Come affrontare il 70% dei fallimenti delle tecniche di PMA? Come …