-
2
-
-
0022966503
-
Post-traumatic hypopituitarism. Six cases and a review of the literature
-
Edwards OM, Clark JD (1986) Post-traumatic hypopituitarism. Six cases and a review of the literature. Medicine (Baltimore) 65: 281-902.
-
(1986)
Medicine (Baltimore)
, vol.65
, pp. 281-902
-
-
Edwards, O.M.1
Clark, J.D.2
-
3
-
-
0031752470
-
Sheehan's syndrome of more than 30 years' duration: An endocrine and MRI study of 6 cases
-
Otsuka F, Kageyama J, Ogura T, Hattori T, Makino H (1998) Sheehan's syndrome of more than 30 years' duration: an endocrine and MRI study of 6 cases. Endocr J 45: 451-458.
-
(1998)
Endocr J
, vol.45
, pp. 451-458
-
-
Otsuka, F.1
Kageyama, J.2
Ogura, T.3
Hattori, T.4
Makino, H.5
-
4
-
-
0023138394
-
Isolated prolactin deficiency in a woman with puerperal alactogenesis
-
Kauppila A, Chatelain P, Kirkinen P, Kivinen S, Ruokonen A (1987) Isolated prolactin deficiency in a woman with puerperal alactogenesis. J Clin Endocrinol Metab 64: 309-312.
-
(1987)
J Clin Endocrinol Metab
, vol.64
, pp. 309-312
-
-
Kauppila, A.1
Chatelain, P.2
Kirkinen, P.3
Kivinen, S.4
Ruokonen, A.5
-
5
-
-
0031003241
-
Familial puerperal alactogenesis: Possibility of a genetically transmitted isolated prolactin deficiency
-
Zargar AH, Masoodi SR, Laway BA, Shah NA, Salahudin M (1997) Familial puerperal alactogenesis: possibility of a genetically transmitted isolated prolactin deficiency. Br J Obstet Gynaecol 104: 629-631.
-
(1997)
Br J Obstet Gynaecol
, vol.104
, pp. 629-631
-
-
Zargar, A.H.1
Masoodi, S.R.2
Laway, B.A.3
Shah, N.A.4
Salahudin, M.5
-
6
-
-
33947587302
-
A case of isolated prolactin deficiency
-
In Japanese
-
Ozawa M, Oki Y, Nishizawa S, Murakami N, Nakamura H (2001) A case of isolated prolactin deficiency. Nihon Naibunpitsu Gakkai Zasshi 77: 66-68 (In Japanese).
-
(2001)
Nihon Naibunpitsu Gakkai Zasshi
, vol.77
, pp. 66-68
-
-
Ozawa, M.1
Oki, Y.2
Nishizawa, S.3
Murakami, N.4
Nakamura, H.5
-
7
-
-
0026475362
-
Isolated prolactin deficiency: A case report
-
Falk RJ (1992) Isolated prolactin deficiency: a case report. Fertil Steril 58: 1060-1062.
-
(1992)
Fertil Steril
, vol.58
, pp. 1060-1062
-
-
Falk, R.J.1
-
8
-
-
0035097095
-
A woman with isolated prolactin deficiency
-
Douchi T, Nakae M, Yamamoto S, Iwamoto I, Oki T, Nagata Y (2001) A woman with isolated prolactin deficiency. Acta Obstet Gynecol Scand 80: 368-370.
-
(2001)
Acta Obstet Gynecol Scand
, vol.80
, pp. 368-370
-
-
Douchi, T.1
Nakae, M.2
Yamamoto, S.3
Iwamoto, I.4
Oki, T.5
Nagata, Y.6
-
9
-
-
0030978612
-
Lymphocytic adrenohypophysitis and lymphocytic infundibuloneurohypophysitis
-
Hashimoto K, Takao T, Makino S (1997) Lymphocytic adrenohypophysitis and lymphocytic infundibuloneurohypophysitis. Endocr J 44: 1-10.
-
(1997)
Endocr J
, vol.44
, pp. 1-10
-
-
Hashimoto, K.1
Takao, T.2
Makino, S.3
-
10
-
-
0032989717
-
Longitudinal hormonal and pituitary imaging changes in two female with combined pituitary hormone deficiency due to deletion of A301, G302 in the Prop-1 gene
-
Mendonca BB, Osorio MGF, Latronico C, Estefan V, Lo LSS, Arnhold IJP (1999) Longitudinal hormonal and pituitary imaging changes in two female with combined pituitary hormone deficiency due to deletion of A301, G302 in the Prop-1 gene. J Clin Endocrinol Metab 84: 942-945.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 942-945
-
-
Mendonca, B.B.1
Osorio, M.G.F.2
Latronico, C.3
Estefan, V.4
Lo, L.S.S.5
Arnhold, I.J.P.6
-
11
-
-
0031741771
-
Phenotypic variability in familial combined pituitary hormone deficiency caused by a Prop-1 gene mutation resulting in the substitution of Arg-Cys at codon 120 (R120C)
-
Fluck C, Deladoey J, Rutishauser K, Eble A, Marti U, Wu W, Mullis PE (1998) Phenotypic variability in familial combined pituitary hormone deficiency caused by a Prop-1 gene mutation resulting in the substitution of Arg-Cys at codon 120 (R120C). J Clin Endocrinol Metab 83: 3727-3734.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 3727-3734
-
-
Fluck, C.1
Deladoey, J.2
Rutishauser, K.3
Eble, A.4
Marti, U.5
Wu, W.6
Mullis, P.E.7
-
12
-
-
0034038650
-
Combined pituitary hormone deficiency and pituitary hypoplasia due to a mutation of the Pit-1 gene
-
Frisch H, Kim C, Hausler G, Pfaffle R (2000) Combined pituitary hormone deficiency and pituitary hypoplasia due to a mutation of the Pit-1 gene. Clin Endocrinol 52: 661-665.
-
(2000)
Clin Endocrinol
, vol.52
, pp. 661-665
-
-
Frisch, H.1
Kim, C.2
Hausler, G.3
Pfaffle, R.4
-
13
-
-
0022477255
-
ACTH and prolactin deficiency
-
Puig ML, Webb SM, del Pozo C, Espinosa JR, Martinez MJ, de Levia A (1986) ACTH and prolactin deficiency. Acta Endocrinol (Copenh) 111: 296-299.
-
(1986)
Acta Endocrinol (Copenh)
, vol.111
, pp. 296-299
-
-
Puig, M.L.1
Webb, S.M.2
del Pozo, C.3
Espinosa, J.R.4
Martinez, M.J.5
de Levia, A.6
-
14
-
-
0030670222
-
Defective mammopoiesis, but normal hematopoiesis, in mice with a targeted disruption of the prolactin gene
-
Horseman ND, Zhao W, Montecino-Rodriguez E, Tanaka M, Nakashima K, Engle SJ, Smith F, Markoff E, Dorshkind K (1997) Defective mammopoiesis, but normal hematopoiesis, in mice with a targeted disruption of the prolactin gene. EMBO J 16: 6926-6935.
-
(1997)
EMBO J
, vol.16
, pp. 6926-6935
-
-
Horseman, N.D.1
Zhao, W.2
Montecino-Rodriguez, E.3
Tanaka, M.4
Nakashima, K.5
Engle, S.J.6
Smith, F.7
Markoff, E.8
Dorshkind, K.9
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