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Items: 1 to 50 of 346

1.

Lawson Wilkins and my life: part 3.

Migeon CJ.

Int J Pediatr Endocrinol. 2014;2014(Suppl 1):S4. doi: 10.1186/1687-9856-2014-S1-S4. No abstract available.

2.

Lawson Wilkins and my life: part 2.

Migeon CJ.

Int J Pediatr Endocrinol. 2014;2014(Suppl 1):S3. doi: 10.1186/1687-9856-2014-S1-S3. No abstract available.

3.

Lawson Wilkins and my life: part 1.

Migeon CJ.

Int J Pediatr Endocrinol. 2014;2014(Suppl 1):S2. doi: 10.1186/1687-9856-2014-S1-S2. No abstract available.

4.

Novel mutation among two sisters with 17β hydroxysteroid dehydrogenase type 3 deficiency.

Massanyi EZ, Gearhart JP, Kolp LA, Migeon CJ.

Urology. 2013 May;81(5):1069-71. doi: 10.1016/j.urology.2012.12.024. Epub 2013 Jan 30.

PMID:
23375913
5.

Review and management of 46,XY disorders of sex development.

Massanyi EZ, Dicarlo HN, Migeon CJ, Gearhart JP.

J Pediatr Urol. 2013 Jun;9(3):368-79. doi: 10.1016/j.jpurol.2012.12.002. Epub 2012 Dec 29. Review.

PMID:
23276787
6.

Absence of prostatic growth in large cohort of adult female patients with congenital adrenal hyperplasia.

Doherty PJ, Friedman AA, Migeon CJ, Macura KJ, Salmasi AH, Lakshmanan Y.

J Urol. 2012 Oct;188(4 Suppl):1588-95. doi: 10.1016/j.juro.2012.02.029. Epub 2012 Aug 19.

PMID:
22910261
8.

Guidelines for the Development of Comprehensive Care Centers for Congenital Adrenal Hyperplasia: Guidance from the CARES Foundation Initiative.

Auchus RJ, Witchel SF, Leight KR, Aisenberg J, Azziz R, Bachega TA, Baker LA, Baratz AB, Baskin LS, Berenbaum SA, Breault DT, Cerame BI, Conway GS, Eugster EA, Fracassa S, Gearhart JP, Geffner ME, Harris KB, Hurwitz RS, Katz AL, Kalro BN, Lee PA, Alger Lin G, Loechner KJ, Marshall I, Merke DP, Migeon CJ, Miller WL, Nenadovich TL, Oberfield SE, Pass KA, Poppas DP, Lloyd-Puryear MA, Quigley CA, Riepe FG, Rink RC, Rivkees SA, Sandberg DE, Schaeffer TL, Schlussel RN, Schneck FX, Seely EW, Snyder D, Speiser PW, Therrell BL, Vanryzin C, Vogiatzi MG, Wajnrajch MP, White PC, Zuckerman AE.

Int J Pediatr Endocrinol. 2010;2010:275213. doi: 10.1155/2010/275213. Epub 2011 Jan 10.

9.

Clinical, genetic, and enzymatic characterization of P450 oxidoreductase deficiency in four patients.

Sahakitrungruang T, Huang N, Tee MK, Agrawal V, Russell WE, Crock P, Murphy N, Migeon CJ, Miller WL.

J Clin Endocrinol Metab. 2009 Dec;94(12):4992-5000. doi: 10.1210/jc.2009-1460. Epub 2009 Oct 16.

10.
11.

Prostate screening in patients with 46,XY disorders of sex development--is it necessary?

Salmasi AH, Wisniewski AB, Novak TE, Gearhart JP, Migeon CJ, Lakshmanan Y.

J Urol. 2008 Oct;180(4):1422-5; discussion 1425-6. doi: 10.1016/j.juro.2008.06.043. Epub 2008 Aug 16.

PMID:
18710761
13.

Medical and psychosexual outcome in women affected by complete gonadal dysgenesis.

McCarty BM, Migeon CJ, Meyer-Bahlburg HF, Zacur H, Wisniewski AB.

J Pediatr Endocrinol Metab. 2006 Jul;19(7):873-7.

PMID:
16995566
14.

Cognitive outcome in adult women affected by congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Malouf MA, Migeon CJ, Carson KA, Petrucci L, Wisniewski AB.

Horm Res. 2006;65(3):142-50. Epub 2006 Feb 28.

PMID:
16508325
15.

Long-term corticosteroid replacement and bone mineral density in adult women with classical congenital adrenal hyperplasia.

King JA, Wisniewski AB, Bankowski BJ, Carson KA, Zacur HA, Migeon CJ.

J Clin Endocrinol Metab. 2006 Mar;91(3):865-9. Epub 2005 Nov 8.

PMID:
16278269
16.

Gender role across development in adult women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Long DN, Wisniewski AB, Migeon CJ.

J Pediatr Endocrinol Metab. 2004 Oct;17(10):1367-73.

PMID:
15526714
17.

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
18.

Psychosexual outcome in women affected by congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Wisniewski AB, Migeon CJ, Malouf MA, Gearhart JP.

J Urol. 2004 Jun;171(6 Pt 1):2497-501.

PMID:
15126884
19.

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
20.

Female phenotype at birth and postnatal masculinization, during the first months of life, associated with transient 5 alpha-reductase 2 deficiency in a preterm infant. A timing defect syndrome?

Vuerich M, Ghirri P, Merusi I, Cuttano A, Baldinotti F, Simi P, Migeon CJ, Boldrini A.

Minerva Pediatr. 2003 Oct;55(5 Suppl 1):82. No abstract available.

PMID:
14992191
21.

Gender assignment in newborns: gender identity/role differentiation in genetic males affected by abnormal sex differentiation.

Migeon CJ.

Minerva Pediatr. 2003 Oct;55(5 Suppl 1):36-40. No abstract available.

PMID:
14992178
22.

Human sex differentiation and its abnormalities.

Migeon CJ, Wisniewski AB.

Best Pract Res Clin Obstet Gynaecol. 2003 Feb;17(1):1-18. Review.

PMID:
12758223
23.
24.

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
25.

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
26.

Gender identity/role differentiation in adolescents affected by syndromes of abnormal sex differentiation.

Wisniewski AB, Migeon CJ.

Adolesc Med. 2002 Feb;13(1):119-28, vii. Review.

PMID:
11841959
27.

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
28.

Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Growth, development, and therapeutic considerations.

Migeon CJ, Wisniewski AB.

Endocrinol Metab Clin North Am. 2001 Mar;30(1):193-206. Review.

PMID:
11344936
29.

Human sex differentiation: from transcription factors to gender.

Migeon CJ, Wisniewski AB.

Horm Res. 2000;53(3):111-9. Review.

PMID:
11044790
30.

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
31.

Sexual differentiation: from genes to gender.

Migeon CJ, Wisniewski AB.

Horm Res. 1998;50(5):245-51. Review.

PMID:
9873191
32.

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
33.

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
34.

The use of adrenalectomy as a treatment for congenital adrenal hyperplasia.

Van Wyk JJ, Gunther DF, Ritzén EM, Wedell A, Cutler GB Jr, Migeon CJ, New MI.

J Clin Endocrinol Metab. 1996 Sep;81(9):3180-90. No abstract available.

PMID:
8784066
35.

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
36.
37.
38.

Human androgen insensitivity due to point mutations encoding amino acid substitutions in the androgen receptor steroid-binding domain.

Murono K, Mendonca BB, Arnhold IJ, Rigon AC, Migeon CJ, Brown TR.

Hum Mutat. 1995;6(2):152-62.

PMID:
7581399
39.

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
40.

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
41.

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
42.

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
44.

Molecular genetics of human androgen insensitivity.

Brown TR, Scherer PA, Chang YT, Migeon CJ, Ghirri P, Murono K, Zhou Z.

Eur J Pediatr. 1993;152 Suppl 2:S62-9. Review.

PMID:
8339746
45.

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
46.

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.

47.

Binding of methyltrienolone to androgen receptors in human skin fibroblasts is enhanced by insulin.

Chang YT, Ghirri P, Migeon CJ, Brown TR.

J Androl. 1992 May-Jun;13(3):242-8.

48.

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
49.

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
50.

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

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