Barry Rich to Humans
This is a "connection" page, showing publications Barry Rich has written about Humans.
Connection Strength
0.066
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An Alu-mediated rearrangement causing a 3.2kb deletion and a novel two base pair deletion in AAAS gene as the cause of triple A syndrome. Mol Genet Metab. 2007 Dec; 92(4):359-63.
Score: 0.010
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Child and parental self-monitoring as determinants of success in the treatment of morbid obesity in low-income minority children. J Pediatr Psychol. 2007 Jan-Feb; 32(1):111-21.
Score: 0.009
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Treatment of morbid obesity in low-income adolescents: effects of parental self-monitoring. Obes Res. 2005 Sep; 13(9):1527-9.
Score: 0.009
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Cardiovascular endurance and heart rate variability in adolescents with type 1 or type 2 diabetes. Biol Res Nurs. 2005 Jul; 7(1):16-29.
Score: 0.009
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Self-reported social class, self-management behaviors, and the effect of diabetes mellitus in urban, minority young people and their families. Arch Pediatr Adolesc Med. 2003 Sep; 157(9):919-25.
Score: 0.008
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Long-term evaluation of multi-disciplinary treatment of morbid obesity in low-income minority adolescents: La Rabida Children's Hospital's FitMatters program. J Adolesc Health. 2006 Oct; 39(4):553-61.
Score: 0.002
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Obesity at the onset of diabetes in an ethnically diverse population of children: what does it mean for epidemiologists and clinicians? Pediatrics. 2005 May; 115(5):e553-60.
Score: 0.002
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Plasma androgens in women with acne vulgaris. J Invest Dermatol. 1983 Jul; 81(1):70-4.
Score: 0.002
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Bioactive luteinizing hormone pituitary reserves during normal and abnormal male puberty. J Clin Endocrinol Metab. 1982 Jul; 55(1):140-6.
Score: 0.002
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A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2002 Jun; 87(6):2556-63.
Score: 0.002
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Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiency. J Clin Endocrinol Metab. 2002 Jun; 87(6):2611-22.
Score: 0.002
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Adrenarche: changing adrenal response to adrenocorticotropin. J Clin Endocrinol Metab. 1981 Jun; 52(6):1129-36.
Score: 0.002
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Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal diabetes mellitus. J Pediatr. 1999 Jan; 134(1):42-6.
Score: 0.001
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Bone mineral density assessment in children with inflammatory bowel disease. Gastroenterology. 1998 May; 114(5):902-11.
Score: 0.001
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Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 gene. Horm Res. 1998; 49(2):98-102.
Score: 0.001
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Response to challenge with gonadotropin-releasing hormone agonist in a mother and her two sons with a constitutively activating mutation of the luteinizing hormone receptor--a clinical research center study. J Clin Endocrinol Metab. 1996 Oct; 81(10):3802-6.
Score: 0.001
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Adrenarche as a cause of benign pseudopuberty in boys. J Pediatr. 1982 Dec; 101(6):1005-9.
Score: 0.000
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Pubertal presentation of congenital delta 5-3 beta-hydroxysteroid dehydrogenase deficiency. J Clin Endocrinol Metab. 1980 Aug; 51(2):345-53.
Score: 0.000
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LH bioactivity increases more than immunoreactivity during puberty. J Pediatr. 1980 Aug; 97(2):205-13.
Score: 0.000
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Bioactive LH: a test to discriminate true precocious puberty from premature thelarche and adrenarche. J Pediatr. 1980 Aug; 97(2):214-6.
Score: 0.000
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Familial nesidioblastosis: severe neonatal hypoglycemia in two families. J Pediatr. 1979 Jul; 95(1):44-53.
Score: 0.000
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Gonadotropin-releasing hormone infusion test in the distinction of hypopituitary patients from normal subjects. Fertil Steril. 1979 May; 31(5):507-12.
Score: 0.000