Titlebook: Clinical Child Neurology; Mustafa A.M. Salih Book 2020 Springer Nature Switzerland AG 2020 DNA Technology.Evidence-based.Neurogenetic Diag

重要

书目名称Clinical Child Neurology影响因子(影响力)




书目名称Clinical Child Neurology影响因子(影响力)学科排名




书目名称Clinical Child Neurology网络公开度




书目名称Clinical Child Neurology网络公开度学科排名




书目名称Clinical Child Neurology被引频次




书目名称Clinical Child Neurology被引频次学科排名




书目名称Clinical Child Neurology年度引用




书目名称Clinical Child Neurology年度引用学科排名




书目名称Clinical Child Neurology读者反馈




书目名称Clinical Child Neurology读者反馈学科排名

攀登

Assessment and Management of the Child with Cerebral Palsy,n to have a significant effect on the quality of life of individuals across the spectrum of disease severity. The prevalence of CP has been reported to be around 2–2.2/1000 live births in well-resourced countries. Limited data is available from developing countries, but the prevalence of CP has been estimated to be as high as 10/1000 in Africa [3].

Nutrient

harbinger

大约冬季

Communication Disorders in Pediatrics,s to make the best possible clinical decisions and appropriate referrals as needed. The medical practitioners namely pediatric specialists is often the first one consulted about speech and language difficulties and the doctors should avoid . approach as simplistic explanations by saying ‘he’ll grow

Cryptic

Autism Spectrum Disorder,Diagnosis is based on applying DSM-5 and ICD-10 criteria, literature indicate that an expert assessment that is based on international diagnostic criteria is enough for clinical diagnosis and to start intervention plans. Yet administering psychometric tools will provide a more comprehensive assessme

Cryptic

ADHD: Clinical Management,itions that may mimic the condition or co-exist with it, and it can be difficult to find the right medication and titrate it to the optimal dose, which may change over time. Non-medication treatments can be effective for many of the behaviors that accompany AD/HD, but these require education of pare

稀释前

细胞膜

Neurometabolic Disorders, suspected, baseline investigations such as blood gas, glucose, lactate, and ammonia may direct the physician toward the possible etiology of the disease. Further investigations like serum amino acids, acylcarnitine profile, and urine organic acids may pinpoint the diagnosis, which may ultimately be

Harness

https://doi.org/10.1007/978-1-349-03914-2l aspects of development, possible causes, related comorbidities, and needed intervention. There are many genetic and metabolic syndromes that are associated with DD and ID but still remains the majority of cases with unknown cause..Developmental surveillance and screening are essential factors for