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244 results
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Mosaicism for deletion 1p36.33 in a patient with obesity and hyperphagia.
Eugster EA, Berry SA, Hirsch B. Eugster EA, et al. Among authors: berry sa. Am J Med Genet. 1997 Jun 27;70(4):409-12. doi: 10.1002/(sici)1096-8628(19970627)70:4<409::aid-ajmg14>;2-l. Am J Med Genet. 1997. PMID: 9182783
Tyrosinase inhibition due to interaction of homocyst(e)ine with copper: the mechanism for reversible hypopigmentation in homocystinuria due to cystathionine beta-synthase deficiency.
Reish O, Townsend D, Berry SA, Tsai MY, King RA. Reish O, et al. Among authors: berry sa. Am J Hum Genet. 1995 Jul;57(1):127-32. Am J Hum Genet. 1995. PMID: 7611281 Free PMC article.
Cockayne syndrome: review of 140 cases.
Nance MA, Berry SA. Nance MA, et al. Among authors: berry sa. Am J Med Genet. 1992 Jan 1;42(1):68-84. doi: 10.1002/ajmg.1320420115. Am J Med Genet. 1992. PMID: 1308368 Review.
Paris-Trousseau syndrome platelets in a child with Jacobsen's syndrome.
Krishnamurti L, Neglia JP, Nagarajan R, Berry SA, Lohr J, Hirsch B, White JG. Krishnamurti L, et al. Among authors: berry sa. Am J Hematol. 2001 Apr;66(4):295-9. doi: 10.1002/ajh.1061. Am J Hematol. 2001. PMID: 11279643
Clinical and biochemical heterogeneity in females of a large pedigree with ornithine transcarbamylase deficiency due to the R141Q mutation.
Ahrens MJ, Berry SA, Whitley CB, Markowitz DJ, Plante RJ, Tuchman M. Ahrens MJ, et al. Among authors: berry sa. Am J Med Genet. 1996 Dec 18;66(3):311-5. doi: 10.1002/(SICI)1096-8628(19961218)66:3<311::AID-AJMG14>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8985493
Brain anomalies, retardation of mentality and growth, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, ear deformity and deafness, eye hypoplasia, cleft palate, cryptorchidism, and kidney dysplasia/hypoplasia (BRESEK/BRESHECK): new X-linked syndrome?
Reish O, Gorlin RJ, Hordinsky M, Rest EB, Burke B, Berry SA. Reish O, et al. Among authors: berry sa. Am J Med Genet. 1997 Feb 11;68(4):386-90. doi: 10.1002/(sici)1096-8628(19970211)68:4<386::aid-ajmg2>;2-k. Am J Med Genet. 1997. PMID: 9021007
Cardiac conduction improvement in two heterozygotes for primary carnitine deficiency on L-carnitine supplementation.
Sarafoglou K, Tridgell AH, Bentler K, Redlinger-Grosse K, Berry SA, Schimmenti LA. Sarafoglou K, et al. Among authors: berry sa. Clin Genet. 2010 Aug;78(2):191-4. doi: 10.1111/j.1399-0004.2009.01368.x. Epub 2010 Jan 4. Clin Genet. 2010. PMID: 20095986
Medical genetics for clinicians. 2. Prenatal diagnosis, teratogens, oncogenes.
Berry SA. Berry SA. Postgrad Med. 1987 Dec;82(8):107-10, 113-5. doi: 10.1080/00325481.1987.11700078. Postgrad Med. 1987. PMID: 3684817 No abstract available.
Regulation of Spi 2.1 and 2.2 gene expression after turpentine inflammation: discordant responses to IL-6.
Berry SA, Bergad PL, Stolz AM, Towle HC, Schwarzenberg SJ. Berry SA, et al. Am J Physiol. 1999 Jun;276(6):C1374-82. doi: 10.1152/ajpcell.1999.276.6.C1374. Am J Physiol. 1999. PMID: 10362600
Hepatic fatty acid-binding protein mRNA is regulated by growth hormone.
Berry SA, Yoon JB, List J, Seelig S. Berry SA, et al. J Am Coll Nutr. 1993 Dec;12(6):638-42. doi: 10.1080/07315724.1993.10718354. J Am Coll Nutr. 1993. PMID: 8294718
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