Twenty years of recombinant human growth hormone in children: Relevance to pediatric care providers

Clinical Pediatrics

Volumn 46, Issue 4, 2007, Pages 279-286

  Hardin, Dana S ^a   Kemp, Stephen F ^b   Allen, David B ^c  

^a OHIO STATE UNIVERSITY   (United States)

^b UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

^c UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

Growth hormone; Growth hormone deficiency; Idiopathic short stature

Indexed keywords

ESTROGEN; HUMAN GROWTH HORMONE; OXANDROLONE; SOMATOMEDIN;

ADIPOSE TISSUE; ADRENAL INSUFFICIENCY; BONE MINERALIZATION; BRAIN PSEUDOTUMOR; CHRONIC KIDNEY FAILURE; CLINICAL MEDICINE; CLINICAL STUDY; CYSTIC FIBROSIS; DIABETES MELLITUS; DIAGNOSTIC PROCEDURE; DOSE CALCULATION; DRUG CONTAMINATION; DRUG INDICATION; DRUG SAFETY; ENTERITIS; FEMUR EPIPHYSIS; GROWTH DISORDER; GROWTH HORMONE DEFICIENCY; HORMONE SUBSTITUTION; HUMAN; JUVENILE RHEUMATOID ARTHRITIS; LEAN BODY WEIGHT; LONG TERM CARE; MEDICAL ETHICS; PANCREATITIS; PATIENT ASSESSMENT; PATIENT REFERRAL; PATIENT SELECTION; PEDIATRICS; PHYSIOLOGY; PRADER WILLI SYNDROME; PUBERTY; REVIEW; SCOLIOSIS; SHORT STATURE; SIDE EFFECT; SMALL FOR DATE INFANT; TREATMENT DURATION; TREATMENT OUTCOME; TURNER SYNDROME;

ADOLESCENT; ARTHRITIS, JUVENILE RHEUMATOID; CHILD; COST-BENEFIT ANALYSIS; CYSTIC FIBROSIS; HUMAN GROWTH HORMONE; HUMANS; INFLAMMATORY BOWEL DISEASES; PEDIATRICS; PRACTICE GUIDELINES; PRADER-WILLI SYNDROME; RECOMBINANT PROTEINS; TIME FACTORS;

EID: 34247266078     PISSN: 00099228     EISSN: None     Source Type: Journal    
DOI: 10.1177/0009922806293924     Document Type: Review

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