-
1
-
-
0023572107
-
Pathology of the testis in intersex syndromes
-
Rutgers JL, Scully R.E. Pathology of the testis in intersex syndromes. Semin Diagn Pathol 1987; 4: 275-91.
-
(1987)
Semin Diagn Pathol
, vol.4
, pp. 275-291
-
-
Rutgers, J.L.1
Scully, R.E.2
-
2
-
-
0036136829
-
Aetiological diagnosis of male sex ambiguity: A collaborative study
-
Morel Y, Rey R, Teinturier C, Nicolino M, Michel-Calemard L, Mowszowicz I et al. Aetiological diagnosis of male sex ambiguity: a collaborative study. Eur J Pediatr 2002; 161: 49-59.
-
(2002)
Eur J Pediatr
, vol.161
, pp. 49-59
-
-
Morel, Y.1
Rey, R.2
Teinturier, C.3
Nicolino, M.4
Michel-Calemard, L.5
Mowszowicz, I.6
-
3
-
-
0027417145
-
Mullerian inhibiting substance: A gonadal hormone with multiple functions
-
Lee MM, Donahoe PK. Mullerian inhibiting substance: a gonadal hormone with multiple functions. Endocr Rev 1993; 14: 152-64.
-
(1993)
Endocr Rev
, vol.14
, pp. 152-164
-
-
Lee, M.M.1
Donahoe, P.K.2
-
4
-
-
0026336259
-
The androgen insensitivity syndrome (testicular feminization): A clinicopathologic study of 43 cases
-
Rutgers JL, Scully RE. The androgen insensitivity syndrome (testicular feminization): a clinicopathologic study of 43 cases. Int J Gynecol Pathol 1991; 10: 126-44.
-
(1991)
Int J Gynecol Pathol
, vol.10
, pp. 126-144
-
-
Rutgers, J.L.1
Scully, R.E.2
-
5
-
-
0026544312
-
Androgen resistance - The clinical and molecular spectrum
-
Griffin JE. Androgen resistance - The clinical and molecular spectrum. N Engl J Med 1992; 326: 611-8.
-
(1992)
N Engl J Med
, vol.326
, pp. 611-618
-
-
Griffin, J.E.1
-
6
-
-
0029069878
-
Androgen receptor defects: Historical, clinical and molecular perspectives
-
Quigley CA, de Bellis A, Marschke KB, El-Awady MK, Wilson EM, French FS. Androgen receptor defects: historical, clinical and molecular perspectives. Endocr Rev 1995; 16: 271-321.
-
(1995)
Endocr Rev
, vol.16
, pp. 271-321
-
-
Quigley, C.A.1
De Bellis, A.2
Marschke, K.B.3
El-Awady, M.K.4
Wilson, E.M.5
French, F.S.6
-
7
-
-
0036913761
-
Persistence of Mullerian remnants in complete androgen insensitivity syndrome
-
Damiani D, Mascolli M, Almeida MJ, Jaubert F, Fellous M, Dichtchekenian V et al. Persistence of Mullerian remnants in complete androgen insensitivity syndrome. J Pediatr Endocrinol Metab 2003; 15: 1553-6.
-
(2003)
J Pediatr Endocrinol Metab
, vol.15
, pp. 1553-1556
-
-
Damiani, D.1
Mascolli, M.2
Almeida, M.J.3
Jaubert, F.4
Fellous, M.5
Dichtchekenian, V.6
-
9
-
-
0029809798
-
Different phenotypes in a family with androgen insensitivity caused by the same M7801 point mutation in the androgen receptor gene
-
Rodien P, Mebarki F, Mowszowicz I, Chaussain JL, Young J, Morel Y et al. Different phenotypes in a family with androgen insensitivity caused by the same M7801 point mutation in the androgen receptor gene. J Clin Endocrinol Metab 1996; 81: 2994-8.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 2994-2998
-
-
Rodien, P.1
Mebarki, F.2
Mowszowicz, I.3
Chaussain, J.L.4
Young, J.5
Morel, Y.6
-
10
-
-
0033616218
-
Persistence of mullerian derivatives in males
-
Belville C, Josso N, Picard JY. Persistence of mullerian derivatives in males. Am J Med Genet 1999; 89: 218-23.
-
(1999)
Am J Med Genet
, vol.89
, pp. 218-223
-
-
Belville, C.1
Josso, N.2
Picard, J.Y.3
-
11
-
-
0028304515
-
Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences
-
Boucekkine C, Toublanc JE, Abbas N, Chaabouni S, Ouahid S, Semrouni M et al. Clinical and anatomical spectrum in XX sex reversed patients. Relationship to the presence of Y specific DNA-sequences. Clin Endocrinol 1994; 40: 733-42.
-
(1994)
Clin Endocrinol
, vol.40
, pp. 733-742
-
-
Boucekkine, C.1
Toublanc, J.E.2
Abbas, N.3
Chaabouni, S.4
Ouahid, S.5
Semrouni, M.6
-
12
-
-
0032925649
-
The human SRY protein is present in fetal and adult Sertoli cells and germ cells
-
Salas-Cortes L, Jaubert F, Barbaux S, Nessmann C, Bono MR, Fellous M et al. The human SRY protein is present in fetal and adult Sertoli cells and germ cells. Int J Dev Biol 1999; 43: 135-40.
-
(1999)
Int J Dev Biol
, vol.43
, pp. 135-140
-
-
Salas-Cortes, L.1
Jaubert, F.2
Barbaux, S.3
Nessmann, C.4
Bono, M.R.5
Fellous, M.6
-
13
-
-
0035506391
-
Expression of the human SRY protein during development in normal male gonadal and sex-reversed tissues
-
Salas-Cortes L, Jaubert F, Bono MR, Fellous M, Rosemblatt M. Expression of the human SRY protein during development in normal male gonadal and sex-reversed tissues. J Exp Zool 2001; 290: 607-15.
-
(2001)
J Exp Zool
, vol.290
, pp. 607-615
-
-
Salas-Cortes, L.1
Jaubert, F.2
Bono, M.R.3
Fellous, M.4
Rosemblatt, M.5
-
15
-
-
0033709679
-
Occurrence of gonadoblastoma in females with Turner syndrome and Y chromosome material: A population study
-
Gravholt CH, Fedder J, Naeraa RW, Muller J. Occurrence of gonadoblastoma in females with Turner syndrome and Y chromosome material: a population study. J Clin Endocrinol Metab 2000; 85: 3199-202.
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 3199-3202
-
-
Gravholt, C.H.1
Fedder, J.2
Naeraa, R.W.3
Muller, J.4
-
16
-
-
0026710412
-
Familial case with sequence variant in the testis-determining region associated with two sex phenotypes
-
Vilain E, McElreavey K, Jaubert F, Raymond JP, Richaud F, Fellous M. Familial case with sequence variant in the testis-determining region associated with two sex phenotypes. Am J Hum Genet 1992; 50: 1008-11.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 1008-1011
-
-
Vilain, E.1
McElreavey, K.2
Jaubert, F.3
Raymond, J.P.4
Richaud, F.5
Fellous, M.6
-
17
-
-
0027286419
-
Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome
-
Abbas N, McElreavey K, Leconiat M, Vilain E, Jaubert F, Berger R et al. Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome. CR Acad Sci III 1993; 316: 375-83.
-
(1993)
CR Acad Sci III
, vol.316
, pp. 375-383
-
-
Abbas, N.1
McElreavey, K.2
Leconiat, M.3
Vilain, E.4
Jaubert, F.5
Berger, R.6
-
18
-
-
0027972478
-
SRY-negative XX fetus with complete male phenotype
-
Vilain E, Le Fiblec B, Morichon-Delvallez N, Brauner R, Dommergues M, Dumez Y et al. SRY-negative XX fetus with complete male phenotype. Lancet 1994; 343: 240-1.
-
(1994)
Lancet
, vol.343
, pp. 240-241
-
-
Vilain, E.1
Le Fiblec, B.2
Morichon-Delvallez, N.3
Brauner, R.4
Dommergues, M.5
Dumez, Y.6
-
19
-
-
0026742034
-
XY sex reversal associated with a nonsense mutation in SRY
-
McElreavey KD, Vilain E, Boucekkine C, Vidaud M, Jaubert F, Richaud F et al. XY sex reversal associated with a nonsense mutation in SRY. Genomics 1992; 13: 838-40.
-
(1992)
Genomics
, vol.13
, pp. 838-840
-
-
McElreavey, K.D.1
Vilain, E.2
Boucekkine, C.3
Vidaud, M.4
Jaubert, F.5
Richaud, F.6
-
20
-
-
0027946855
-
True hermaphroditism: Genetic variants and clinical management
-
Hadjiathanasiou CG, Brauner R, Lortat-Jacob S, Nivot S, Jaubert F, Fellous M et al. True hermaphroditism: genetic variants and clinical management. J Pediatr 1994; 125: 738-44.
-
(1994)
J Pediatr
, vol.125
, pp. 738-744
-
-
Hadjiathanasiou, C.G.1
Brauner, R.2
Lortat-Jacob, S.3
Nivot, S.4
Jaubert, F.5
Fellous, M.6
-
21
-
-
0034490171
-
SRY protein is expressed in ovotestis and streak gonads from human sex-reversal
-
Salas-Cortes L, Jaubert F, Nihoul-Fékété C, Brauner R, Rosemblatt M, Fellous M. SRY protein is expressed in ovotestis and streak gonads from human sex-reversal. Cytogenet Cell Genet 2000; 91: 212-6.
-
(2000)
Cytogenet Cell Genet
, vol.91
, pp. 212-216
-
-
Salas-Cortes, L.1
Jaubert, F.2
Nihoul-Fékété, C.3
Brauner, R.4
Rosemblatt, M.5
Fellous, M.6
-
22
-
-
0019974331
-
Dysgenesis of testicular and streak gonads in the syndrome of mixed gonadal dysgenesis: Perspective derived from a clinicopathologic analysis of twenty-one cases
-
Robboy SJ, Miller T, Donahoe PK, Jahre C, Welch WR, Haseltine FP et al. Dysgenesis of testicular and streak gonads in the syndrome of mixed gonadal dysgenesis: Perspective derived from a clinicopathologic analysis of twenty-one cases. Hum Pathol 1982; 13: 700-16.
-
(1982)
Hum Pathol
, vol.13
, pp. 700-716
-
-
Robboy, S.J.1
Miller, T.2
Donahoe, P.K.3
Jahre, C.4
Welch, W.R.5
Haseltine, F.P.6
-
23
-
-
0026335160
-
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 et al. Clinical and pathologic spectrum of 46,XY gonadal dysgenesis: its relevance to the understanding of sex differentiation. Medicine 1991; 70: 375-83.
-
(1991)
Medicine
, vol.70
, pp. 375-383
-
-
Berkovitz, G.D.1
Fechner, P.Y.2
Zacur, H.W.3
Rock, J.A.4
Snyder III, H.M.5
Migeon, C.J.6
-
24
-
-
0027216138
-
Mixed gonadal dysgenesis: Clinical, cytogenetic, endocrinological, and histopathological findings in 16 patients
-
Mendez JP, Ulloa-Aguirre A, Kofman-Alfaro S, Mutchinick O, Fernandez-del-Castillo C, Reyes E et al. Mixed gonadal dysgenesis: clinical, cytogenetic, endocrinological, and histopathological findings in 16 patients. Am J Med Genet 1993; 46: 263-7.
-
(1993)
Am J Med Genet
, vol.46
, pp. 263-267
-
-
Mendez, J.P.1
Ulloa-Aguirre, A.2
Kofman-Alfaro, S.3
Mutchinick, O.4
Fernandez-Del-Castillo, C.5
Reyes, E.6
-
25
-
-
0029864920
-
Testicular dysgenesis does not affect expression of anti-mullerian hormone by Sertoli cells in premeiotic seminiferous tubules
-
Rey R, al-Attar L, Louis F, Jaubert F, Barbet P, Nihoul- Fékété C et al. Testicular dysgenesis does not affect expression of anti-mullerian hormone by Sertoli cells in premeiotic seminiferous tubules. Am J Pathol 1996; 148: 1689-98.
-
(1996)
Am J Pathol
, vol.148
, pp. 1689-1698
-
-
Rey, R.1
Al-Attar, L.2
Louis, F.3
Jaubert, F.4
Barbet, P.5
Nihoul- Fékété, C.6
-
26
-
-
0023139581
-
Complete and incomplete Drash syndrome: A clinicopathologic study of five cases of a dysontogenetic-neoplastic complex
-
Manivel JC, Sibley RK, Dehner LP. Complete and incomplete Drash syndrome: a clinicopathologic study of five cases of a dysontogenetic-neoplastic complex. Hum Pathol 1987; 18: 80-9.
-
(1987)
Hum Pathol
, vol.18
, pp. 80-89
-
-
Manivel, J.C.1
Sibley, R.K.2
Dehner, L.P.3
-
27
-
-
0037242419
-
Surgical management and genotype/phenotype correlations in WT1 gene-related diseases (Drash, Frasier syndromes)
-
Auber F, Lortat-Jacob S, Sarnacki S, Jaubert F, Salomon R, Thibaud E et al. Surgical management and genotype/phenotype correlations in WT1 gene-related diseases (Drash, Frasier syndromes). J Pediatr Surg 2003; 38: 124-9.
-
(2003)
J Pediatr Surg
, vol.38
, pp. 124-129
-
-
Auber, F.1
Lortat-Jacob, S.2
Sarnacki, S.3
Jaubert, F.4
Salomon, R.5
Thibaud, E.6
-
28
-
-
16944365351
-
Donor splice-site mutations in WT1 are responsible for Frasier syndrome
-
Barbaux S, Niaudet P, Gubler MC, Grunfeld JP, Jaubert F, Kuttenn F et al. Donor splice-site mutations in WT1 are responsible for Frasier syndrome. Nat Genet 1997; 17: 467-70.
-
(1997)
Nat Genet
, vol.17
, pp. 467-470
-
-
Barbaux, S.1
Niaudet, P.2
Gubler, M.C.3
Grunfeld, J.P.4
Jaubert, F.5
Kuttenn, F.6
-
29
-
-
0032913826
-
The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor
-
Barbosa AS, Hadjiathanasiou CG, Theodoridis C, Papathanasiou A, Tar A, Merksz M et al. The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor. Hum Mutat 1999; 13: 146-53.
-
(1999)
Hum Mutat
, vol.13
, pp. 146-153
-
-
Barbosa, A.S.1
Hadjiathanasiou, C.G.2
Theodoridis, C.3
Papathanasiou, A.4
Tar, A.5
Merksz, M.6
-
30
-
-
0033365196
-
Sex chromosome genetics '99: Gonadoblastoma, testicular and prostate cancers, and the TSPY gene
-
Lau YFC. Sex chromosome genetics '99: Gonadoblastoma, testicular and prostate cancers, and the TSPY gene. Am J Hum Genet 1999; 64: 921-7.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 921-927
-
-
Lau, Y.F.C.1
-
31
-
-
0023091256
-
Abnormal sexual differentiation and neoplasia
-
Verp MS, Simpson JL. Abnormal sexual differentiation and neoplasia. Cancer Genet Cytogenet 1987; 25: 191-218.
-
(1987)
Cancer Genet Cytogenet
, vol.25
, pp. 191-218
-
-
Verp, M.S.1
Simpson, J.L.2
-
32
-
-
0023203241
-
Placental alkaline phosphatase immunoreactivity in testicular germ-cell neoplasms
-
Manivel JC, Jessurun J, Wick MR, Dehner LP. Placental alkaline phosphatase immunoreactivity in testicular germ-cell neoplasms. Am J Surg Pathol 1987; 11: 21-9.
-
(1987)
Am J Surg Pathol
, vol.11
, pp. 21-29
-
-
Manivel, J.C.1
Jessurun, J.2
Wick, M.R.3
Dehner, L.P.4
-
33
-
-
0031040644
-
Heterogeneity of gonadoblastoma germ cells: Similarities with immature germ cells, spermatogonia and testicular carcinoma in situ cells
-
Jorgensen N, Müller J, Jaubert F, Clausen OP, Skakkebaek NE. Heterogeneity of gonadoblastoma germ cells: similarities with immature germ cells, spermatogonia and testicular carcinoma in situ cells. Histopathology 1997; 30: 177-86.
-
(1997)
Histopathology
, vol.30
, pp. 177-186
-
-
Jorgensen, N.1
Müller, J.2
Jaubert, F.3
Clausen, O.P.4
Skakkebaek, N.E.5
-
34
-
-
0026351240
-
Morphology and immunohistochemistry of carcinoma in situ adjacent to testicular germ cell tumours in adults and children: Implications for histogenesis
-
Soosay GN, Bobrow L, Happerfield L, Parkinson MC. Morphology and immunohistochemistry of carcinoma in situ adjacent to testicular germ cell tumours in adults and children: implications for histogenesis. Histopathology 1991; 19: 537-44.
-
(1991)
Histopathology
, vol.19
, pp. 537-544
-
-
Soosay, G.N.1
Bobrow, L.2
Happerfield, L.3
Parkinson, M.C.4
-
35
-
-
0030957528
-
The prepubertal testis (prenatal and postnatal): Its relationship to intratubular germ cell neoplasia: A combined Pediatric Oncology Group and Children's Cancer Study Group
-
Hawkins E, Heifetz SA, Giller R, Cushing B. The prepubertal testis (prenatal and postnatal): its relationship to intratubular germ cell neoplasia: a combined Pediatric Oncology Group and Children's Cancer Study Group. Hum Pathol 1997; 28: 404-10.
-
(1997)
Hum Pathol
, vol.28
, pp. 404-410
-
-
Hawkins, E.1
Heifetz, S.A.2
Giller, R.3
Cushing, B.4
-
36
-
-
0022442742
-
Structures mimicking sex cord-stromal tumours and gonadoblastomas in the ovaries of normal infants and children
-
Safneck JR, deSa DJ. Structures mimicking sex cord-stromal tumours and gonadoblastomas in the ovaries of normal infants and children. Histopathology 1986; 10: 909-20.
-
(1986)
Histopathology
, vol.10
, pp. 909-920
-
-
Safneck, J.R.1
DeSa, D.J.2
-
37
-
-
0023766547
-
Ovarian tumorlike structures, biovular follicles, and binucleated oocytes in children: Their frequency and possible pathologic significance
-
Manivel JC, Dehner LP, Burke B. Ovarian tumorlike structures, biovular follicles, and binucleated oocytes in children: their frequency and possible pathologic significance. Pediatr Pathol 1988; 8: 283-92.
-
(1988)
Pediatr Pathol
, vol.8
, pp. 283-292
-
-
Manivel, J.C.1
Dehner, L.P.2
Burke, B.3
-
38
-
-
0033518280
-
Leydig-cell tumors caused by an activating mutation of the gene encoding the luteinizing hormone receptor
-
Liu G, Duranteau L, Carel JC, Monroe J, Doyle DA, Shenker A. Leydig-cell tumors caused by an activating mutation of the gene encoding the luteinizing hormone receptor. N Engl J Med 1999; 341: 1731-6.
-
(1999)
N Engl J Med
, vol.341
, pp. 1731-1736
-
-
Liu, G.1
Duranteau, L.2
Carel, J.C.3
Monroe, J.4
Doyle, D.A.5
Shenker, A.6
-
39
-
-
0023921596
-
The testicular "tumor" of the adrenogenital syndrome. A report of six cases and review of the literature on testicular masses in patients with adrenocortical disorders
-
Rutgers JL, Young RH, Scully RE. The testicular "tumor" of the adrenogenital syndrome. A report of six cases and review of the literature on testicular masses in patients with adrenocortical disorders. Am J Surg Pathol 1988; 12: 503-13.
-
(1988)
Am J Surg Pathol
, vol.12
, pp. 503-513
-
-
Rutgers, J.L.1
Young, R.H.2
Scully, R.E.3
-
40
-
-
0037348617
-
Dax1 regulates testis cord organization during gonadal differentiation
-
Meeks JJ, Crawford SE, Russell TA, Morohashi K, Weiss J, Jameson JL. Dax1 regulates testis cord organization during gonadal differentiation. Development 2003; 130: 1029-36.
-
(2003)
Development
, vol.130
, pp. 1029-1036
-
-
Meeks, J.J.1
Crawford, S.E.2
Russell, T.A.3
Morohashi, K.4
Weiss, J.5
Jameson, J.L.6
-
41
-
-
18444375272
-
Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses
-
Vialard F, Ottolenghi C, Gonzales M, Choiset A, Girard S, Siffroi JP et al. Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses. J Med Genet 2002; 39: 514-8.
-
(2002)
J Med Genet
, vol.39
, pp. 514-518
-
-
Vialard, F.1
Ottolenghi, C.2
Gonzales, M.3
Choiset, A.4
Girard, S.5
Siffroi, J.P.6
-
42
-
-
1242352080
-
Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients
-
Domenice S, Correa RV, Costa EMF, Nishi MY, Vilain E, Arnhold IJP et al. Mutations in the SRY, DAX1, SF1 and WNT4 genes in Brazilian sex-reversed patients. Braz J Med Biol Res 2004; 37: 145-50.
-
(2004)
Braz J Med Biol Res
, vol.37
, pp. 145-150
-
-
Domenice, S.1
Correa, R.V.2
Costa, E.M.F.3
Nishi, M.Y.4
Vilain, E.5
Arnhold, I.J.P.6
|