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Gerli - Die Hexe vom Moor. Life is a Story - story.one
Auf meinen Streifzügen durch die Natur begegnete mir Gerli, die Hexe vom Moor. Ein wunderbarer Austausch entstand. Sie erzählte vom Wirken der Menschen in der Region und von der Weisheit unserer Ahnen. Sie lehrte mich, dass der Blick nach innen - die Sicht in die Welt weiten kann. Sie lehrte mich, dass mein Herz viele Antworten kennt.
JIMD Reports, Volume 37
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
Reducing Complexity: Explaining Inborn Errors of Metabolism and Their Treatment to Children and Adolescents
Abstract: Background Inborn errors of metabolism (IEM) are a group of rare, heterogeneous and complex genetic conditions. Clinically, IEM often affect the central nervous system and other organs. Some carry the risk of progression and / or potentially life-threatening crises. Many patients have to adhere to lifelong dietary or drug treatment. The complexity of IEM makes it difficult for patients and caregivers to understand their pathophysiology, inheritance and therapy rationale. Especially patients reaching adolescence may have only limited knowledge of their condition since medical care has often entirely been handled by their parents. Knowledge about disease and treatment, however, const...
JIMD Reports, Volume 31
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
Sternstunden. Life is a Story - story.one
Sternstunden des Lebens bleiben für immer.
Auf der Suche nach dem Licht. Life is a Story - story.one
Ich war eine Suchende. Bis der Tag kam, an dem ich erkannte, dass mich das Leben findet.
JIMD Reports, Volume 20
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
JIMD Reports, Volume 21
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
JIMD Reports, Volume 45
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
JIMD Reports, Volume 29
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
