BackgroundIn recent decades, considerable progress in diagnosis and treatment of patients with intoxication-type inborn errors of metabolism (IT-IEM) such as urea cycle disorders (UCD), organic acidurias (OA), maple syrup urine disease (MSUD), or tyrosinemia type 1 (TYR 1) has resulted in a growing group of long-term survivors. However, IT-IEM still require intense patient and caregiver effort in terms of strict dietetic and pharmacological treatment, and the threat of metabolic crises is always present. Furthermore, crises can affect the central nervous system (CNS), leading to cognitive, behavioural and psychiatric sequelae. Consequently, the well-being of the patients warrants consideration from both a medical and a psychosocial viewpoin...
Organic acidurias (OAs), urea‐cycle disorders (UCDs), and maple syrup urine disease (MSUD) belong to...
Inborn errors of metabolism (IEMs) are characterized by deficits in metabolic enzymes as a result of...
Background: Inborn errors of metabolism (IEM) form an important cause of movement disorders in child...
INTRODUCTION Progress in diagnosis and treatment of patients with intoxication-type inborn errors o...
BACKGROUND Organic acidurias (OADs) and urea cycle disorders (UCDs) are inborn metabolic disorders ...
Acute intoxication-type inborn errors of metabolism (IT-IEM) such as urea cycle disorders and non-ac...
Background Living with a non-acute (phenylketonuria) or acute (e.g. urea cycle disorders, organic...
INTRODUCTION This study is part of the "European network and registry for intoxication type metaboli...
Background: Inborn errors of metabolism (IEMs) refer to rare heterogeneous genetic disorders with va...
Inborn errors of metabolism (IEMs) refer to rare heterogeneous genetic disorders with various clinic...
OBJECTIVE: It is important for psychiatrists to be aware of certain inborn errors of metabolism (IEM...
Background: Inborn errors of metabolism (IEM) form an important cause of movement disorders in child...
Inherited disorders of neurotransmitter metabolism are a group of rare diseases, which are caused by...
Inborn errors of metabolism (IEMs) are characterized by deficits in metabolic enzymes as a result of...
Organic acidurias (OAs), urea‐cycle disorders (UCDs), and maple syrup urine disease (MSUD) belong to...
Inborn errors of metabolism (IEMs) are characterized by deficits in metabolic enzymes as a result of...
Background: Inborn errors of metabolism (IEM) form an important cause of movement disorders in child...
INTRODUCTION Progress in diagnosis and treatment of patients with intoxication-type inborn errors o...
BACKGROUND Organic acidurias (OADs) and urea cycle disorders (UCDs) are inborn metabolic disorders ...
Acute intoxication-type inborn errors of metabolism (IT-IEM) such as urea cycle disorders and non-ac...
Background Living with a non-acute (phenylketonuria) or acute (e.g. urea cycle disorders, organic...
INTRODUCTION This study is part of the "European network and registry for intoxication type metaboli...
Background: Inborn errors of metabolism (IEMs) refer to rare heterogeneous genetic disorders with va...
Inborn errors of metabolism (IEMs) refer to rare heterogeneous genetic disorders with various clinic...
OBJECTIVE: It is important for psychiatrists to be aware of certain inborn errors of metabolism (IEM...
Background: Inborn errors of metabolism (IEM) form an important cause of movement disorders in child...
Inherited disorders of neurotransmitter metabolism are a group of rare diseases, which are caused by...
Inborn errors of metabolism (IEMs) are characterized by deficits in metabolic enzymes as a result of...
Organic acidurias (OAs), urea‐cycle disorders (UCDs), and maple syrup urine disease (MSUD) belong to...
Inborn errors of metabolism (IEMs) are characterized by deficits in metabolic enzymes as a result of...
Background: Inborn errors of metabolism (IEM) form an important cause of movement disorders in child...