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Items: 1 to 50 of 70

1.

Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD.

Seeherunvong T, Ukarapong S, McElreavey K, Berkovitz GD, Perera EM.

J Pediatr Endocrinol Metab. 2012;25(1-2):121-3.

PMID:
22570960
2.

Megakaryocyte development is normal in mice with targeted disruption of Tescalcin.

Ukarapong S, Bao Y, Perera EM, Berkovitz GD.

Exp Cell Res. 2012 Mar 10;318(5):662-9. doi: 10.1016/j.yexcr.2012.01.009. Epub 2012 Jan 18.

PMID:
22285131
3.

Madelung-like deformity in pseudohypoparathyroidism type 1b.

Sanchez J, Perera E, Jan de Beur S, Ding C, Dang A, Berkovitz GD, Levine MA.

J Clin Endocrinol Metab. 2011 Sep;96(9):E1507-11. doi: 10.1210/jc.2011-1411. Epub 2011 Jul 13.

4.

Expression and evolutionary conservation of the tescalcin gene during development.

Bao Y, Hudson QJ, Perera EM, Akan L, Tobet SA, Smith CA, Sinclair AH, Berkovitz GD.

Gene Expr Patterns. 2009 Jun;9(5):273-81. doi: 10.1016/j.gep.2009.03.004. Epub 2009 Apr 2.

PMID:
19345287
5.

A nine year old girl with thyrotoxicosis, ataxia, and chorea.

Seeherunvong T, Diamantopoulos S, Berkovitz GD.

Brain Dev. 2007 Nov;29(10):660-1. Epub 2007 May 23.

PMID:
17524583
6.

Sex determination, differentiation, and identity.

Migeon CJ, Berkovitz GD, Wisniewski AB.

N Engl J Med. 2004 May 20;350(21):2204-6; author reply 2204-6. No abstract available.

PMID:
15156589
7.

46,XX sex reversal with partial duplication of chromosome arm 22q.

Seeherunvong T, Perera EM, Bao Y, Benke PJ, Benigno A, Donahue RP, Berkovitz GD.

Am J Med Genet A. 2004 Jun 1;127A(2):149-51.

PMID:
15108202
8.

Attitudes of adult 46, XY intersex persons to clinical management policies.

Meyer-Bahlburg HF, Migeon CJ, Berkovitz GD, Gearhart JP, Dolezal C, Wisniewski AB.

J Urol. 2004 Apr;171(4):1615-9; discussion 1619.

PMID:
15017234
9.

Genetic mechanisms that regulate testis determination.

Carrillo AA, Berkovitz GD.

Rev Endocr Metab Disord. 2004 Mar;5(1):77-82. Review. No abstract available.

PMID:
14966391
10.

Characterization of tescalcin, a novel EF-hand protein with a single Ca2+-binding site: metal-binding properties, localization in tissues and cells, and effect on calcineurin.

Gutierrez-Ford C, Levay K, Gomes AV, Perera EM, Som T, Kim YM, Benovic JL, Berkovitz GD, Slepak VZ.

Biochemistry. 2003 Dec 16;42(49):14553-65.

PMID:
14661968
11.

46,XY intersex individuals: phenotypic and etiologic classification, knowledge of condition, and satisfaction with knowledge in adulthood.

Migeon CJ, Wisniewski AB, Brown TR, Rock JA, Meyer-Bahlburg HF, Money J, Berkovitz GD.

Pediatrics. 2002 Sep;110(3):e32.

PMID:
12205282
12.

Ambiguous genitalia with perineoscrotal hypospadias in 46,XY individuals: long-term medical, surgical, and psychosexual outcome.

Migeon CJ, Wisniewski AB, Gearhart JP, Meyer-Bahlburg HF, Rock JA, Brown TR, Casella SJ, Maret A, Ngai KM, Money J, Berkovitz GD.

Pediatrics. 2002 Sep;110(3):e31.

PMID:
12205281
13.

Congenital micropenis: long-term medical, surgical and psychosexual follow-up of individuals raised male or female.

Wisniewski AB, Migeon CJ, Gearhart JP, Rock JA, Berkovitz GD, Plotnick LP, Meyer-Bahlburg HF, Money J.

Horm Res. 2001;56(1-2):3-11.

PMID:
11815721
14.

Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis.

Ottolenghi C, Moreira-Filho C, Mendonça BB, Barbieri M, Fellous M, Berkovitz GD, McElreavey K.

J Clin Endocrinol Metab. 2001 Jun;86(6):2465-9.

PMID:
11397841
15.

Mutation analysis of subjects with 46, XX sex reversal and 46, XY gonadal dysgenesis does not support the involvement of SOX3 in testis determination.

Lim HN, Berkovitz GD, Hughes IA, Hawkins JR.

Hum Genet. 2000 Dec;107(6):650-2. Epub 2000 Nov 14. Erratum in: Hum Genet. 2004 Aug;115(3):263.

PMID:
11153920
16.

Tescalcin, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, Col9a3, and renin are expressed in the mouse testis during the early stages of gonadal differentiation.

Perera EM, Martin H, Seeherunvong T, Kos L, Hughes IA, Hawkins JR, Berkovitz GD.

Endocrinology. 2001 Jan;142(1):455-63.

PMID:
11145610
17.

Complete androgen insensitivity syndrome: long-term medical, surgical, and psychosexual outcome.

Wisniewski AB, Migeon CJ, Meyer-Bahlburg HF, Gearhart JP, Berkovitz GD, Brown TR, Money J.

J Clin Endocrinol Metab. 2000 Aug;85(8):2664-9.

PMID:
10946863
18.

Prenatal diagnosis of Smith-Lemli-Opitz syndrome in a pregnancy with low maternal serum oestriol and a sex-reversed fetus.

Bick DP, McCorkle D, Stanley WS, Stern HJ, Staszak P, Berkovitz GD, Meyers CM, Kelley RI.

Prenat Diagn. 1999 Jan;19(1):68-71. Review.

PMID:
10073912
19.

Abnormalities of gonadal differentiation.

Berkovitz GD, Seeherunvong T.

Baillieres Clin Endocrinol Metab. 1998 Apr;12(1):133-42. Review.

PMID:
9890065
20.

Growth hormone excess in a child with neurofibromatosis type 1 and optic pathway tumor: a patient report.

Fuqua JS, Berkovitz GD.

Clin Pediatr (Phila). 1998 Dec;37(12):749-52. No abstract available.

PMID:
9864651
21.

Evaluation of boys with marked breast development at puberty.

Sher ES, Migeon CJ, Berkovitz GD.

Clin Pediatr (Phila). 1998 Jun;37(6):367-71. Review.

PMID:
9637901
22.

Molecular investigation of two male subjects with short stature and a 45,X/46,X,ring(Y) karyotype.

Sher ES, Addelston MB, Plotnick L, Urban MD, Berkovitz GD.

Horm Res. 1998;49(1):46-50.

PMID:
9438785
23.

Analysis of the SRY gene in gonadal tissue of subjects with 46,XY gonadal dysgenesis.

Fuqua JS, McLaughlin J, Perlman EJ, Berkovitz GD.

J Clin Endocrinol Metab. 1997 Feb;82(2):701-2. No abstract available.

PMID:
9024280
24.

Linkage analysis of a kindred with inherited 46,XY partial gonadal dysgenesis.

Fuqua JS, Sher ES, Fechner PY, Ostrer H, Oddeux C, Schafer AJ, Rosales TO, Migeon CJ, Berkovitz GD.

J Clin Endocrinol Metab. 1996 Dec;81(12):4479-83.

PMID:
8954063
25.

Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination.

McElreavey K, Vilain E, Barbaux S, Fuqua JS, Fechner PY, Souleyreau N, Doco-Fenzy M, Gabriel R, Quereux C, Fellous M, Berkovitz GD.

Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8590-4.

26.

Mutation analysis of the 2 kb 5' to SRY in XY females and XY intersex subjects.

Kwok C, Tyler-Smith C, Mendonca BB, Hughes I, Berkovitz GD, Goodfellow PN, Hawkins JR.

J Med Genet. 1996 Jun;33(6):465-8.

27.

Abnormal gonadal differentiation in two subjects with ambiguous genitalia, Mullerian structures, and normally developed testes: evidence for a defect in gonadal ridge development.

Fuqua JS, Sher ES, Perlman EJ, Urban MD, Ghahremani M, Pelletier J, Migeon CJ, Brown TR, Berkovitz GD.

Hum Genet. 1996 Apr;97(4):506-11.

PMID:
8834252
28.
29.

Combined Leydig cell and Sertoli cell dysfunction in 46,XX males lacking the sex determining region Y gene.

Turner B, Fechner PY, Fuqua JS, Marcantonio SM, Perlman EJ, Vordermark JS, Berkovitz GD.

Am J Med Genet. 1995 Jul 3;57(3):440-3.

PMID:
7677147
30.

Abnormalities of thyroid function and glucose control in subjects with Rett syndrome.

Cooke DW, Naidu S, Plotnick L, Berkovitz GD.

Horm Res. 1995;43(6):273-8.

PMID:
7607612
31.

Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditism.

Fechner PY, Rosenberg C, Stetten G, Cargile CB, Pearson PL, Smith KD, Migeon CJ, Berkovitz GD.

Cytogenet Cell Genet. 1994;66(1):22-6.

PMID:
8275702
32.

Embryonic testicular regression sequence: a part of the clinical spectrum of 46,XY gonadal dysgenesis.

Marcantonio SM, Fechner PY, Migeon CJ, Perlman EJ, Berkovitz GD.

Am J Med Genet. 1994 Jan 1;49(1):1-5.

PMID:
8172233
33.

Report of a kindred with X-linked (or autosomal dominant sex-limited) 46,XY partial gonadal dysgenesis.

Fechner PY, Marcantonio SM, Ogata T, Rosales TO, Smith KD, Goodfellow PN, Migeon CJ, Berkovitz GD.

J Clin Endocrinol Metab. 1993 May;76(5):1248-53. Review.

PMID:
8496317
34.

The role of the sex-determining region Y gene in the etiology of 46,XX maleness.

Fechner PY, Marcantonio SM, Jaswaney V, Stetten G, Goodfellow PN, Migeon CJ, Smith KD, Berkovitz GD, Amrhein JA, Bard PA, et al.

J Clin Endocrinol Metab. 1993 Mar;76(3):690-5.

PMID:
8383144
35.

The effect of epidermal growth factor in human granulosa cells varies with follicle size.

Hurst BS, Zacur HA, Schlaff WD, Damewood MD, Berkovitz GD.

J Endocrinol Invest. 1993 Feb;16(2):143-5.

PMID:
8463551
36.

Hypocalcemia in nonwhite breast-fed infants. Vitamin D deficiency revisited.

Chang YT, Germain-Lee EL, Doran TF, Migeon CJ, Levine MA, Berkovitz GD.

Clin Pediatr (Phila). 1992 Nov;31(11):695-8. No abstract available.

PMID:
1424401
37.

Evidence for increased prevalence of SRY mutations in XY females with complete rather than partial gonadal dysgenesis.

Hawkins JR, Taylor A, Goodfellow PN, Migeon CJ, Smith KD, Berkovitz GD.

Am J Hum Genet. 1992 Nov;51(5):979-84.

38.

Abnormalities of gonadal determination and differentiation.

Berkovitz GD.

Semin Perinatol. 1992 Oct;16(5):289-98. Review. No abstract available.

PMID:
1485186
39.

Use of granulosa-luteal cell culture to evaluate low and high clinical responses to menotropin stimulation.

Hurst BS, Zacur HA, Schlaff WD, Berkovitz GD.

J Endocrinol Invest. 1992 Sep;15(8):567-72.

PMID:
1430840
40.

Partial gonadal dysgenesis in a patient with a marker Y chromosome.

Fechner PY, Smith KD, Jabs EW, Migeon CJ, Berkovitz GD.

Am J Med Genet. 1992 Apr 1;42(6):807-12.

PMID:
1313209
41.

Induction and superinduction of messenger ribonucleic acid specific for aromatase cytochrome P-450 in cultured human skin fibroblasts.

Berkovitz GD, Chen S, Migeon CJ, Levine MA.

J Clin Endocrinol Metab. 1992 Mar;74(3):629-34.

PMID:
1740498
42.

The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism.

Berkovitz GD, Fechner PY, Marcantonio SM, Bland G, Stetten G, Goodfellow PN, Smith KD, Migeon CJ.

Hum Genet. 1992 Feb;88(4):411-6.

PMID:
1740318
43.

DNA binding activity of recombinant SRY from normal males and XY females.

Harley VR, Jackson DI, Hextall PJ, Hawkins JR, Berkovitz GD, Sockanathan S, Lovell-Badge R, Goodfellow PN.

Science. 1992 Jan 24;255(5043):453-6.

PMID:
1734522
44.

Clinical and pathologic spectrum of 46,XY gonadal dysgenesis: its relevance to the understanding of sex differentiation.

Berkovitz GD, Fechner PY, Zacur HW, Rock JA, Snyder HM 3rd, Migeon CJ, Perlman EJ.

Medicine (Baltimore). 1991 Nov;70(6):375-83.

PMID:
1956279
45.

Endocrine evaluation of adults with mild hypospadias.

Gearhart JP, Donohoue PA, Brown TR, Walsh PC, Berkovitz GD.

J Urol. 1990 Aug;144(2 Pt 1):274-7.

PMID:
2115596
46.

Abnormal induction of aromatase activity by dexamethasone in fibroblasts from a patient with cortisol resistance.

Berkovitz GD, Carter KM, Levine MA, Migeon CJ.

J Clin Endocrinol Metab. 1990 Jun;70(6):1608-11.

PMID:
2347895
47.

Testosterone lowers aromatase activity in cultured human genital skin fibroblasts.

Berkovitz GD, Carter KM, Brown TR, Migeon CJ.

Mol Cell Endocrinol. 1990 Mar 5;69(2-3):187-97.

PMID:
2328827
48.

Influence of cell culture conditions on aromatase activity in human genital skin fibroblasts.

Bisat T, Brown TR, Migeon CJ, Berkovitz GD.

In Vitro Cell Dev Biol. 1989 Sep;25(9):806-12.

PMID:
2793780
49.

Aromatase activity in microsomal preparations of human genital skin fibroblasts: influence of glucocorticoids.

Berkovitz GD, Bisat T, Carter KM.

J Steroid Biochem. 1989 Sep;33(3):341-7.

PMID:
2779225
50.

Serum 3 alpha-androstanediol glucuronide measurements in sexually mature women with congenital adrenal hyperplasia during therapy.

Reiner BJ, Donohoue PA, Migeon CJ, Berkovitz GD.

J Clin Endocrinol Metab. 1989 Jul;69(1):105-9.

PMID:
2732292

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