نتایج جستجو برای: infantile apparent life

تعداد نتایج: 864776  

Journal: :Pediatric annals 2012
Stan L Block

The etiology of infantile failure to thrive in the US is extremely diverse. Causes range from naive or malevolent parents; cost of formula for low-income families; mothers inexperienced with breast-feeding; and a range of organic causes. Many experts categorize failure-tothrive (FTT) as either organic or nonorganic. Recognizing the initial stages of FTT is challenging, but becomes readily appar...

پایان نامه :دانشگاه آزاد اسلامی - دانشگاه آزاد اسلامی واحد تهران مرکزی - دانشکده مدیریت 1390

در کشور ما از سالها پیش انواع بیمه های زندگی ارائه می شد لکن استقبال مردم از این بیمه ها بسیار پایین بود.در چند سال اخیر طرح جدیدی از بیمه های زندگی با الگو برداری از بیمه نامه ای به نام universal life insurance که شرکتهای بیمه در دنیا به خصوص کشورهای غربی عرضه می کنند،ارائه گردیده است. با ارائه این بیمه نامه درایران،فروش آن در سالهای اخیر رشد قابل توجهی داشته است لکن هنوز میزان استقبال ازاین ب...

Journal: :JAMA 2013
Silvia Romanello Daniele Spiri Elena Marcuzzi Anna Zanin Priscilla Boizeau Simon Riviere Audrey Vizeneux Raffaella Moretti Ricardo Carbajal Jean-Christophe Mercier Chantal Wood Gian Vincenzo Zuccotti Giovanni Crichiutti Corinne Alberti Luigi Titomanlio

IMPORTANCE Infantile colic is a common cause of inconsolable crying during the first months of life and has been thought to be a pain syndrome. Migraine is a common cause of headache pain in childhood. Whether there is an association between these 2 types of pain in unknown. OBJECTIVE To investigate a possible association between infantile colic and migraines in childhood. DESIGN, SETTING, ...

Journal: :Pediatrics 2008
Linda C Chang Anita N Haggstrom Beth A Drolet Eulalia Baselga Sarah L Chamlin Maria C Garzon Kimberly A Horii Anne W Lucky Anthony J Mancini Denise W Metry Amy J Nopper Ilona J Frieden

OBJECTIVES Infantile hemangiomas often are inapparent at birth and have a period of rapid growth during early infancy followed by gradual involution. More precise information on growth could help predict short-term outcomes and make decisions about when referral or intervention, if needed, should be initiated. The objective of this study was to describe growth characteristics of infantile heman...

2009
Eileen E. Birch Jingyun Wang

Purpose—To review what is known about the normal maturation of stereoacuity, the stereoacuity deficits associated with infantile and accommodative esotropia, the rationale for making improved stereoacuity a goal of treatment, and strategies for improving stereoacuity outcomes. Methods—Studies of stereoacuity maturation during normal development, studies of stereoacuity outcomes following treatm...

Journal: :Journal of tropical pediatrics 2015
Asburçe Olgaç Leyla Tümer Öznur Boyunağa Metehan Kızılkaya Alev Hasanoğlu

Osteopetrosis is a rare genetic condition of reduced osteoclastic bone resorption which causes defective bone remodeling and skeletal sclerosis during growth, having effects on many organs and tissues. Mutation of T-cell immune regulator 1 (TCRG1) gene is the most common genetic defect leading to osteopetrosis, with poor prognosis. The autosomal recessive form presents in the infantile period (...

Journal: :The Journal of nutrition 2012
Janina R Galler Cyralene P Bryce Miriam L Zichlin Garrett Fitzmaurice G David Eaglesfield Deborah P Waber

Infantile malnutrition is known to be associated with cognitive and behavioral impairment during childhood and adolescence. Data pertaining to longer-term effects on behavioral outcomes in adulthood are limited. In this study, we report associations between infantile malnutrition and attention problems in adults at midlife. Attention problems were assessed by the Conners Adult ADHD Rating Scale...

2015
Asburçe Olgaç Leyla Tümer Öznur Boyunağa Metehan Kızılkaya Alev Hasanoğlu

Osteopetrosis is a rare genetic condition of reduced osteoclastic bone resorption which causes defective bone remodeling and skeletal sclerosis during growth, having effects on many organs and tissues. Mutation of T-cell immune regulator 1 (TCRG1) gene is the most common genetic defect leading to osteopetrosis, with poor prognosis. The autosomal recessive form presents in the infantile period (...

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