Gonadal differentiation-Normal and abnormal testicular development

Advances in Experimental Medicine and Biology

Volumn 511, Issue , 2002, Pages 15-23

  Hadziselimovic, Faruk ^a   Huff, Dale ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GONADOTROPIN; MUELLERIAN INHIBITING FACTOR; TESTOSTERONE;

ADOLESCENT; ADULT; ANDROGEN INSENSITIVITY SYNDROME; CHILD; CLINICAL FEATURE; CONFERENCE PAPER; CRYPTORCHISM; DISEASE ASSOCIATION; EMBRYO; FEMALE; FETUS; GENE EXPRESSION; GONADAL DYSGENESIS; GONADOBLASTOMA; HISTOPATHOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPOTHALAMUS HYPOPHYSIS GONAD SYSTEM; INFANT; KARYOTYPE 47,XXY; KLINEFELTER SYNDROME; LEYDIG CELL; MAJOR CLINICAL STUDY; MALE; MALE INFERTILITY; MALE PSEUDOHERMAPHRODITISM; NOONAN SYNDROME; PERSISTENT MULLERIAN DUCT SYNDROME; PHENOTYPE; PREPUBERTY; PRIORITY JOURNAL; PUBERTY; SEMINIFEROUS TUBULE; SEMINOMA; SERTOLI CELL; SEX CHROMOSOME MOSAICISM; SEX DIFFERENTIATION; SEX DIFFERENTIATION DISORDER; SPERMATOCYTE; SPERMATOGENESIS; SPERMATOGONIUM; TESTIS; TESTIS TUMOR; TISSUE SECTION; TREATMENT INDICATION;

EID: 0036922185     PISSN: 00652598     EISSN: None     Source Type: Journal    
DOI: 10.1007/978-1-4615-0621-8_2     Document Type: Article

References (23)

1. Aiman J, Griffin JE. The frequency of androgen receptor deficiency in infertile men. J Clin Endocrinol Metab 54:725-732, 1982.
2. Brown TR, Scherer PA, Chang Ying-Tai, Migeon CI, Ghirri P, Murano K, Zhou F. Molecular genetics of human androgen insensitivity. Eur J Pediatr 152:(Suppl 2) S62-69, 1993.
3. Cate RL, Mattaliano RJ, Hession C, et al. Isolation of the bovine and the human genes for Müllerian inhibiting substance and expression of the human gene in animal cells. Cell 45:685-689, 1986.
4. Forest MG, Sizonenko PC, Cathiard AM, and Bertrand J. Hypophyso-gonadal function in humans during the first year of life. 1. Evidence for testicular activity in early infancy. J Clin Invest 53:819, 1974.
5. Gendrel D, Job JC, and Roger M. Reduced post-natal rise of testosterone in plasma of cryptorchid infants. Acta Endocr 89:372, 1978.
6. Grumbach MM, Roth JC, Kaplan SL, and Kelch RP. Hypothalamic-pituitary regulation of puberty: evidence and concepts derived from clinical research, in: The Control of the Onset of Puberty. MM Grumbach, GD Grave, FE Mayer., eds., John Wiley and Sons, New York, Chapter 6, pp. 115-181, 1974.
7. Grumbach M, Conte F. Disorders of sex differentiation, in: Williams Textbook of Endocrinology, J Wilson, D Foster, eds., Saunders, 1998.
8. Guerrier D, Tran D, Vanderwinden JM et al. The persistent Müllerian duct syndrome: a molecular approach. J Clin Endocrinol Metab 68:46-52, 1989.
9. Hadziselimovic F. Funktionelle Morphologie des kindlichen Hodens im ersten Lebensjahr. Acta Anat 99:342 abstract 378, 1977.
10. Hadziselimovic F. Cryptorchidism: Ultrastructure of Normal and Cryptorchid Testis Development. New York, Springer-Verlag, 1977.
11. Hadziselimovic F. Cryptorchidism: Management and Implications. New York: Springer-Verlag, 1983.
12. Hadziselimovic F, Thommen L, Girard J, and Herzog B. The significance of postnatal gonadotropin surge for testicular development in normal and cryptorchid testes. J Urol 136:274-276, 1986.
13. Hedinger C, Dhom G. Pathologie des mänlichen Genitale. Springer Verlag Berlin, Heidelberg pp. 70-100, 1991.
14. Imbeaud S, Rey R, Berta P, et al. Testicular degeneration in three patients with the persistent Müllerian duct syndrome. Eur J Pediatr 154:187-190, 1995.
15. Josso N, Picard JY, Imbeaud S, Carrė-Eusèbe D, Zeller J, Adamsbaum C. The persistent Müllerian duct syndromne: a rare cause of cryptorchidism. Eur J Pediatr 152:(Suppl 2) S76-S78, 1993.
16. Loeff D, Imbeaud S, Reyes HM, et al. Surgical and genetic aspects of persistent Müllerian duct syndrome. J Pediatr Surg 29:61-65, 1994.
17. MacLaughlin DT, Epstein J, Donahoe PK. Bioassay, purification, cloning, and expression of Müllerian inhibiting substance. Methods in Enzymology 198:358-369, 1991.
18. Müller J. Morphometery and Histology of gonads from twelve children and adolscents with the androgen insensitivity (testicular feminization) syndrome. J Clin Endocr Metab 59:785-789, 1984.
19. Nachtigal MW, Ingraham HA. Bioactivation of Müllerian inhibiting substance during gonadal develpment by a kex2/subtilisin-like endoprotease. Proc Am Acad Sci USA 93:7711-7716, 1996.
20. Rutgers JL, Scully RE. Pathology of the testis in intersex syndromes. Semin Diegn Pathol 4:275-291, 1987.
21. Siebeman R. Die Gonadendysgenesien: Klinefeltersyndrom, Tumersyndrom und echter Hermaphroditismus. Vivchows Arch [A] 331:417-440, 1958.
22. Winter JSD, Hughes I, Reyes FI, and Faiman C. Pituitary-gonadal relations in infancy: 2. Patterns of serum gonadal steroid concentrations in man from birth to two years of age. J Clin Endocr Metab 42:679, 1976.
23. Zang KD. Genetics and cytogenetics of Klinefelter's syndrome, in: Klinefelter Syndrome, HJ Baudmann, R Brut, E Perwein, eds., Springer Verlag, New York, pp 12-23, 1991.