KovacsKHorvathE: Tumours of the pituitary gland. In: HartmanWH (ed): Atlas tumour of pathology. Armed Forces Institute of Pathology, Washington DC1986: 1–264 (vol fascicle XXI).
HallWALucianoMG: Pituitary magnetic resonance imaging in normal human volunteers: occult adenomas in the general population. Ann Intern Med120: 817–820, 1994.
7.
MindermannTWilsonCB: Age-related and gender-related occurrence of pituitary adenomas [published erratum appears in Clin Endocrinol (Oxf) 41(5): 700, 1994]. Clin Endocrinol (Oxf)41: 359–364, 1994.
SpadaAArosioM: Clinical, biochemical and morphological correlates in patients bearing growth hormone-secreting pîtuitary tumours with or without constitutively active adenylate cyclase. J Clin Endocrinol Metab71:1421–1426, 1990.
WolpertSM: The radiology of pituitary adenomas. Endocrinol Metab Clin North Am16: 553–584, 1987.
31.
OldfieldEHChrousosGP: Preoperative lateralization of ACTH-secreting pituitary microadenomas by bilateral and simultaneous inferior petrosal venous sinus sampling. N Engl J Med312: 100–103, 1985.
32.
ThaparKKovacsK: Pituitary adenomas: current concepts in classification, histopathology, and molecular biology. The Endocrinologist3: 39–56, 1993.
33.
HardyJ: Transsphenoidal surgery of hypersecreting pitutary tumours. In: KohlerPORossGT (eds): Diagnosis and treatment of pituitary tumours. Excerpta Medica, Amsterdam1973: 179–194.
34.
MolitchMEThornerMOWilsonC: Management of prolactinomas. J Clin Endocrinol Metab82: 996–1000, 1997.
35.
MolitchME: Pituitary adenomas [letter; comment]. Ann Intern Med122: 476, 1995.
36.
KlibanskiAZervasNT: Diagnosis and management of hormone-secreting pituitary adenomas. N Engl J Med324: 822–831, 1991.
37.
LawsERJr: Pituitary surgery. Endocrinol Metab Clin North Am16, 1987.
WilsonCB: A decade of pituitary microsurgery. J Neurosurg61: 814–833, 1984.
44.
ChunMMaskoGBHetelekidisS: Radiotherapy in the treatment of pituitary adenomas. Int J Radiat Oncol Biol Phys15: 305–309, 1988.
45.
GrigsbyPWStokesS: Prognostic factors and results of radiotherapy alone in the management of pituitary adenomas. Int J Radiat Oncol Biol Phys15: 1103–1110, 1988.
46.
ShelineGTyrrellJ: Pituitary tumours. In: PerezCBradyL (eds): Principles and practice of radiation oncology. JB Lippincott Co, Philadelphia, PA1987: 1108–1125.
47.
NelsonPBGoodmanML: Endocrine function in patients with large pituitary tumours treated with operative decompression and radiation therapy. Neurosurgery24: 398–400, 1989.
48.
SnyderPJFowbleBF: Hypopituitarism following radiation therapy of pituitary adenomas. Am J Med81: 457–462, 1986.
49.
BradaMFordD: Risk of second brain tumour after conservative surgery and radiotherapy for pituitary adenoma. BMJ304: 1343–1346, 1992.
50.
LittleyMDShaletSM: Hypopituitarism following external radiotherapy for pituitary tumours in adults. Q J Med262:145–160, 1989.
51.
LinfootJA: Heavy ion therapy. In: LinfootJA (ed): Recent advances in the diagnosis and treatment of pituitary tumours. Raven Press, New York, NY1979: 245–268.
52.
EastmanRCGordenP: Radiation therapy of acromegaly. Endocrinol Metab Clin North Am21: 693–712, 1992.
53.
ConstineLSWoolfPD: Hypothalamic-pituitary dysfunction after radiation for brain tumours. N Engl J Med328: 87–94, 1993.
54.
BradaMRajanB: The long-term efficacy of conservative surgery and radiotherapy in the control of pituitary adenomas. Clin Endocrinol38: 571–578, 1993.
BarkanALHalaszI: Pituitary irradiation is ineffective in normalizing plasma insulin-like growth factor I in patients with acromegaly [see comments]. J Clin Endocrinol Metab82: 3187–3191, 1997.
57.
ThorénMRähnT: Stereotactic radiosurgery with the cobalt-60 gamma unit in the treatment of growth hormone-producing pituitary tumours. Neurosurgery29: 663–668, 1991.
58.
PollockBEKondziolkaD: Stereotactic radiosurgery for pituitary adenomas: imaging, visual and endocrine results. Acta Neurochir Suppl (Wien)62: 33–38, 1994.
59.
ShelineGE. Proceedings: Treatment of nonfunctioning chromophobe adenomas of the pituitary. Am J Roentgenol Radium Ther Nucl Med120: 553–561, 1974.
60.
TsangRWLaperriereNJ: Glioma arising after radiation therapy for pituitary adenoma. A report of four patients and estimation of risk [published erratum appears in Cancer 73(2): 492, 1994]. Cancer72: 2227–2233, 1993.
61.
ThornerMVanceML: The anterior pituitary. In: WilsonJDFosterDW (eds): Williams Textbook of Endocrinology. WB Saunders, Philadelphia, PA1998: 249–340.
62.
LambertsSWHoflandLJ: Octreotide and related somatostatin analogs in the diagnosis and treatment of pituitary disease and somatostatin receptor scintigraphy. Front Neuroendocrinol14: 27–55, 1993.
63.
LambertsSWvan der LelyAJ: Octreotide. N Engl J Med334: 246–254, 1996.
64.
VanceMLEvansWSThornerMO: Drugs five years later. Bromocriptine. Ann Intern Med100: 78–91, 1984.
65.
LiuzziADallabonzanaD: Low doses of dopamine agonists in the long-term treatment of macroprolactinomas. N Engl J Med313: 656–659, 1985.
MolitchME: Pregnancy and the hyperprolactinemic woman. N Engl J Med312: 1364–1370, 1985.
68.
KupersmithMJRosenbergCKleinbergD: Visual loss in pregnant women with pituitary adenomas [see comments]. Ann Intern Med121: 473–477, 1994.
69.
GemzellCWangCF: Outcome of pregnancy in women with pituitary adenoma. Fertil Steril31: 363–372, 1979.
70.
van't VerlaatJWCroughsRJBrownellJ: Treatment of macroprolactinomas with a new non-ergot, long-acting dopaminergic drug, CV 205-502. Clin Endocrinol (Oxf)33: 619–624, 1990.
71.
DuranteauLChansonP: Effect of the new dopaminergic agonist CV 205–502 on plasma prolactin levels and tumour size in bromocriptine-resistant prolactinomas. Clin Endocrinol (Oxf)34: 25–29, 1991.
72.
BrueTPellegriniI: Effects of the dopamine agonist CV 205–502 in human prolactinomas resistant to bromocriptine. J Clin Endocrinol Metab74: 577–584, 1992.
73.
VilarLBurkeCW: Quinagolide efficacy and tolerability in hyperprolactinaemic patients who are resistant to or intolerant of bromocriptine [see comments]. Clin Endocrinol (Oxf)41: 821–826, 1994.
74.
RainsCPBrysonHMFittonA: Cabergoline: a review of its pharmacological properties and therapeutic potential in the treatment of hyperprolactinæmia and inhibition of lactation. Drugs49: 255–279, 1995.
75.
WebsterJPiscitelliG: A comparison of cabergoline and bromocriptine in the treatment of hyperprolactinemic amenorrhea. Cabergoline Comparative Study Group [see comments]. N Engl J Med331: 904–909, 1994.
76.
BillerBMMolitchME: Treatment of prolactin-secreting macroadenomas with the once-weekly dopamine agonist cabergoline. J Clin Endocrinol Metab81: 2338–2343, 1996.
77.
ColaoADi SarnoA: Prolactinomas resistant to standard dopamine agonists respond to chronic cabergoline treatment [see comments]. J Clin Endocrinol Metab82: 876–883, 1997.
78.
ColaoADi SarnoA: Long-term and low-dose treatment with cabergoline induces macroprolactinoma shrinkage. J Clin Endocrinol Metab82: 3574–3579, 1997.
79.
JaffeCABarkanAL: Treatment of acromegaly with dopamine agonists. Endocrinol Metab Clin North Am21: 713–735, 1992.
80.
MillerJWCrapoL: The medical treatment of Cushing's syndrome. Endocr Rev14: 443–458, 1993.
81.
ChansonPTimsitJHarrisAG: Clinical pharmacokinetics of octreotide. Therapeutic applications in patients with pituitary tumours. Clin Pharmacokinet25: 375–391, 1993.
82.
SassolasGHarrisAGJames-DeidierA: Long term effect of incremental doses of the somatostatin analog SMS 201–995 in 58 acromegalic patients. French SMS 201–995 Acromegaly Study Group. J Clin Endocrinol Metab71: 391–397, 1990.
83.
VanceMLHarrisAG: Long-term treatment of 189 acromegalic patients with the somatostatin analog octreotide. Results of the International Multicenter Acromegaly Study Group. Arch Intern Med151:1573–1578, 1991.
84.
EzzatSSnyderPJ: Octreotide treatment of acromegaly. A randomized, multicenter study. Ann Intern Med117:711–718, 1992.
85.
NewmanCBMelmedS: Safety and efficacy of long-term octreotide therapy of acromegaly: results of a multicenter trial in 103 patients—a clinical research center study [published erratum appears in J Clin Endocrinol Metab 80(11): 3238, 1995]. J Clin Endocrinol Metab80: 2768–2775, 1995.
86.
GillisJCNobleSGoaKL: Octreotide long-acting release (LAR). A review of its pharmacological properties and therapeutic use in the management of acromegaly. Drugs53: 681–699, 1997.
87.
HeronIThomasF: Pharmacokinetics and efficacy of a long-acting formulation of the new somatostatin analog BIM 23014 in patients with acromegaly. J Clin Endocrinol Metab76: 721–727, 1993.
88.
MorangeIDe BoisvilliersF: Slow release lanreotide treatment in acromegalic patients previously normalized by octreotide. J Clin Endocrinol Metab79:145–151, 1994.
89.
GiustiMGussoniG: Effectiveness and tolerability of slow release lanreotide treatment in active acromegaly: six-month report on an Italian multicenter study. Italian Multicenter Slow Release Lanreotide Study Group [see comments]. J Clin Endocrinol Metab81: 2089–2097, 1996.
90.
CaronPMorange-RamosI: Three year follow-up of acromegalic patients treated with intramuscular slow-release lanreotide [see comments]. J Clin Endocrinol Metab82: 18–22, 1997.
91.
ChansonPWeintraubBDHarrisAG: Octreotide therapy for thyroid-stimulating hormone-secreting pituitary adenomas. A follow-up of 52 patients. Ann Intern Med119: 236–240, 1993.
92.
GancelAVuillermetP: Effects of a slow-release formulation of the new somatostatin analogue lanreotide in TSH-secreting pituitary adenomas. Clin Endocrinol (Oxf)40: 421–428, 1994.
93.
WarnetATimsitJ: The effect of somatostatin analogue on chiasmal dysfunction from pituitary macroadenomas. J Neurosurg71: 687–690, 1989.
94.
WarnetAHarrisAG: A prospective multicenter trial of octreotide in 24 patients with visual defects caused by nonfunctioning and gonadotropin-secreting pituitary adenomas. Neurosurgery41: 786–797, 1997.
95.
KrenningEPKwekkeboomDJ: Somatostatin receptor scintigraphy with [111In-DTPA-D-Phe1]- and [123I-Tyr3]-octreotide: the Rotterdam experience with more than 1000 patients. Eur J Nucl Med20: 716–731, 1993.
96.
ChansonP: Predicting the effects of long-term medical treatment in acromegaly. At what cost? For what benefits? [comment]. Eur J Endocrinol136: 359–361, 1997.
97.
EbersoldMJQuastLM: Long-term results in transsphenoidal removal of nonfunctioning pituitary adenomas. J Neurosurg64: 713–719, 1986.
98.
HarrisPEAfsharF: The effects of transsphenoidal surgery on endocrine function and visual fields in patients with functionless pituitary tumours. Q J Med71: 417–427, 1989.
99.
ComtoisRBeauregardH: The clinical and endocrine outcome to transphenoidal microsurgery of non secreting pituitary adenomas. Cancer68: 860–866, 1991.
HayesTPDavisRARaventosA: The treatment of pituitary chromophobe adenomas. Radiology98: 149–153, 1971.
102.
CiricIMikhaelM: Transsphenoidal microsurgery of pituitary macroadenomas with long-term follow-up results. J Neurosurg59: 395–401, 1983.
103.
VlahovitchBReynaudC: Treatment and recurrences in 135 pituitary adenomas. Acta Neurochir42 (Suppl): 120–123, 1988.
104.
Jaffrain-ReaMLDeromeP: Influence of radiotherapy on long-term relapse in clinically non- secreting pituitary adenomas. A retrospective study (1970–1988). Eur J Med2: 398–403, 1993.
105.
BradleyKMAdamsCBT: An audit of selected patients with non-functioning pituitary adenoma treated by transsphenoidal surgery without irradiation. Clin Endocrinol41: 655–659, 1994.
106.
GittoesNJLBatesAS: Radiotherapy for non-functioning pituitary tumours. Clinical Endocrinology48: 331–337, 1998.
107.
RosenTBengtssonA-G: Premature mortality due to cardiovascular disease in hypopituitarism. Lancet336: 285–288, 1990.
108.
BatesASVan't HoffW: The effects of hypopituitarism on life expectancy. J Clin Endocrinol Metab81: 1169–1172, 1996.
109.
BülowBHagmarL: Increased cerebrovascular mortality in patients with hypopituitarism. Clin Endocrinol46: 75–81, 1997.
BuchfelderMFahlbuschR: Neurosurgical treatment of Cushing's disease in children and adolescents. Acta Neurochir Suppl (Wien)35: 101–105, 1985.
119.
LosaMOecklerR: Evaluation of selective transsphenoidal adenomectomy by endocrinological testing and somatomedin-C measurement in acromegaly. J Neurosurg70: 561–567, 1989.
120.
LambergBAKivikangasV: Conventional pituitary irradiation in acromegaly. Effect on growth hormone and TSH secretion. Acta Endocrinol (Copenh)82: 267–281, 1976.
121.
FeekCMMcLellandJ: How effective is external pituitary irradiation for growth hormone- secreting pituitary tumours?Clin Endocrinol (Oxf)20: 401–408, 1984.
122.
KlimanBKjellbergRN: Long-term effects of proton-beam therapy for acromegaly. In: RobbinsRJMelmedS (eds): Acromegaly. Plenum Press, New York1986: 221–228.
123.
SpeirsCJReedPI: The effectiveness of external beam radiotherapy for acromegaly is not affected by previous pituitary ablative treatments. Acta Endocrinol (Copenh)122: 559–565, 1990.
124.
ChansonPGrellier-FouquerayP: Comment et avec quelle efficacité traite-t-on l'acromégalie en 1997? Enquête transversale sur une population de 74 acromégales (Abst). Ann Endocrinol (Paris)58 (Suppl 2): 2S69, 1997.
125.
ArosioMMacchelliS: Effects of treatment with octreotide in acromegalic patients - a multicenter Italian study. Italian Multicenter Octreotide Study Group. Eur J Endocrinol133: 430–439, 1995.
126.
FløgstadAKHalseJ: Sandostatin LAR in acromegalic patients: long-term treatment [see comments]. J Clin Endocrinol Metab82: 23–28, 1997.
127.
LancranjanIBrunsC: Sandostatin LAR: a promising therapeutic tool in the management of acromegalic patients. Metabolism45: 67–71, 1996.
128.
StewartPMKaneKF: Depot long-acting somatostatin analog (Sandostatin-LAR) is an effective treatment for acromegaly. J Clin Endocrinol Metab80: 3267–3272. 1995.
129.
FeigenbaumSLDowneyDE: Transsphenoidal pituitary resection for preoperative diagnosis of prolactin-secreting pituitary adenoma in women: long term follow-up. J Clin Endocrinol Metab81: 1711–1719, 1996.
130.
ThomsonJADaviesDL: Ten year follow up of microprolactinoma treated by transsphenoidal surgery. Bmj309: 1409–1410, 1994.
131.
SerriOHardyJMassoudF: Relapse of hyperprolactinemia revisited [letter]. N Engl J Med329: 1357, 1993.
132.
GrossmanACohenBL: Treatment of prolactinomas with megavoltage radiotherapy. Br Med J (Clin Res Ed)288: 1105–1109, 1984.
TsagarakisSGrossmanA: Megavoltage pituitary irradiation in the management of prolactinomas: long-term follow-up. Clin Endocrinol (Oxf)34: 399–406, 1991.
135.
ArnottRDPestellRG: A critical evaluation of transsphenoidal surgery in the treatment of Cushing's disease: prediction of outcome. Acta Endocrinol (Copenh.)123: 423–430, 1990.
136.
BochicchioDLosaMBuchfelderM: Factors influencing the immediate and late outcome of Cushing's disease treated by transsphenoidal surgery: a retrospective study by the European Cushing's Disease Survey Group [see comments]. J Clin Endocrinol Metab80: 3114–3120, 1995.
137.
GuilhaumeBBertagnaX: Transsphenoidal pituitary surgery for the treatment of Cushing's disease: results in 64 patients and long term follow-up studies. J Clin Endocrinol Metab66: 1056–1064, 1988.
138.
MampalamTJTyrrellJBWilsonCB: Transsphenoidal microsurgery for Cushing disease. A report of 216 cases. Ann Intern Med109: 487–493, 1988.
139.
BurkeCWAdamsCB: Transsphenoidal surgery for Cushing's disease: does what is removed determine the endocrine outcome?Clin Endocrinol (Oxf)33: 525–537, 1990.
140.
PostKDHabasJE: Comparison of long term results between prolactin secreting adenomas and ACTH secreting adenomas. Can J Neurol Sci17: 74–77, 1990.
141.
TindallGTHerringCJ: Cushing's disease: results of transsphenoidal microsurgery with emphasis on surgical failures. J Neurosurg72: 363–369, 1990.
142.
RobertFHardyJ: Cushing's disease: a correlation of radiological, surgical and pathological findings with therapeutic results. Pathol Res Pract187: 617–621, 1991.
TrainerPJLawrieHS: Transsphenoidal resection in Cushing's disease: undetectable serum cortisol as the definition of successful treatment [see comments]. Clin Endocrinol (Oxf)38: 73–78, 1993.
145.
RamZNiemanLK: Early repeat surgery for persistent Cushing's disease. J Neurosurg80: 37–45, 1994.
146.
StyneDMGrumbachMM: Treatment of Cushing's disease in childhood and adolescence by transsphenoidal microadenomectomy. N Engl J Med310: 889–893, 1984.
147.
DyerEHCivitT: Transsphenoidal surgery for pituitary adenomas in children. Neurosurgery34: 207–212; discussion 212, 1994.
148.
LeinungMCKaneLA: Long term follow-up of transsphenoidal surgery for the treatment of Cushing's disease in childhood. J Clin Endocrinol Metab80: 2475–2479, 1995.
149.
MagiakouMAMastorakosG: Cushing's syndrome in children and adolescents. Presentation, diagnosis, and therapy. N Engl J Med331: 629–636, 1994.
150.
HowlettTAPlowmanPN: Megavoltage pituitary irradiation in the management of Cushing's disease and Nelson's syndrome: long-term follow-up. Clin Endocrinol (Oxf)31:309–323, 1989.
151.
EstradaJBoronatM: The long-term outcome of pituitary irradiation after unsuccessful transsphenoidal surgery in Cushing's disease [see comments]. N Engl J Med336: 172–177, 1997.
152.
TyrrellJBWilsonCB: Cushing's disease. Therapy of pituitary adenomas. Endocrinol Metab Clin North Am23: 925–938, 1994.
153.
EtxabeJVazquezJA: Morbidity and mortality in Cushing's disease: an epidemiological approach. Clin Endocrinol (Oxf)40: 479–484, 1994.
154.
De BoerHBlokGJvan der VeenEA: Clinical aspects of growth hormone in adults. Endocrine Rev16: 63–86, 1995.
155.
MelmedS: The Pituitary. Blackwell Science, Boston, MA1995.