P47 |
Forced
conservative management of a patient with pituitary tumour apoplexy
and reduced conscious level |
|
A Advani, RA James, A Jenkins, JH Parr, J
Scott, R Cooper & ST Wahid |
P48 |
An
unusual presentation of 'fits' |
|
S Dissanayake, M Lazdam, V Basker, A Fryer,
RC Strange, M Deaken & F Hanna |
P49 |
An
unusual cause of confusion |
|
A Tahrani & P Moulik |
P50 |
Recurrent
congenital neonatal hyperthyroidism in a mother with Graves' disease
(post radio-ablation) on thyroxine replacement |
|
J Kumar, P Rajendran, R Lapworth, C Buchanan & C
Williams |
P51 |
Isolated
ACTH deficiency following long-term benzodiazepine treatment |
|
K Müssig, E Friess, K Mörike, H-U
Häring & D Overkamp |
P52 |
Infertility
and bilateral testicular masses due to 21-hydroxylase deficiency |
|
K Müssig, S Kaltenbach, C Maser-Gluth,
MF Hartmann, SA Wudy, M Horger, B Gallwitz, F Raue, H-U Häring & E
Schulze |
P53 |
Graves'
eye disease following radioiodine treatment for toxic nodular goitre |
|
A Tahrani & P Moulik |
P54 |
Recurrent
hypoglycaemia: an unusual association of islet cell hyperplasia
and coeliac disease |
|
RS Moisey, D Wright & SR Peacey |
P55 |
Screening
of osteoporosis in a small Romanian town |
|
S Mandasescu & MM Trisca |
P56 |
Acute
myocardial infarction and Graves' thyrotoxicosis |
|
RA Chudleigh, PJD Owen, S Bhattachrya & JS
Davies |
P57 |
Acromegaly,
pregnancy and diabetes mellitus - a successful maternal and foetal
outcome |
|
SS Seshadri, D Wright, DC Whitelaw & SR
Peacey |
P58 |
Surgical
management of metastatic phaeochromocytoma: review of 2 cases |
|
TH El-Tawil, KH Darzy, R Carpenter, S Bhattacharya,
S Edmondson & JP Monson |
P59 |
The
coincidence of mucoepidermoid and papillary thyroid carcinoma.
A case report |
|
GL Kovacs, F Salamon, Z Gorombey, L Kovacs,
E Hubina, MI Goth & I Szabolcs |
P60 |
DIre
Straits - hypothalamic diabetes insipidus, acute myeloid leukaemia
and high risk cytogenetics: 45,XX,t(3;3)(q21q26),-7 |
|
KS Myint, M Besser, J Craig, D Halsall, H
Simpson, DF Wood, VKK Chatterjee & M Gurnell |
P61 |
Metastatic
insulinoma or not? |
|
KS Myint, RK Semple, I MacFarlane, D Appleton,
RK Praseedom, H Simpson, DF Wood, VKK Chatterjee & M Gurnell |
P62 |
APECED
(autoimmune polyendocrinopathycandidiasis- ectodermal dystrophy)
syndrome with atypical or incomplete presentation: report of 4
cases with AIRE gene mutations in heterozygosity |
|
C Mazza, I Sparapani, L Costa, S Zanola,
M Filisetti, A Pilotta, F Lombardi, MI Spagnuolo, G Valerio, A
Franzese, G Radetti & F Buzi |
P63 |
Relationship
between age of onset, natural course and therapeutic approach in
patients with acromegaly |
|
EI Marova, VS Pronin, SE Agadzanjan, NN Molitvoslovova,
MB Antsiferov & TM Alexeeva |
P64 |
Sweet's
syndrome and thyroid diseases: is there a link? |
|
F Magri, E Gabellieri, AR Sorrentino, MI
Rizza, L Chiovato & E Ferrari |
P65 |
Bone
marrow hypoplasia in a patient with panhypopituitarism responsive
to sex hormone therapy. The importance of compliance with testosterone
therapy |
|
MA Badawi, FS Farah, MY Elkhalifa, A Al-Humaidi & TA
Elhadd |
P66 |
Multiple
endocrine neoplasia type 1 (MEN1) in a patient with systemic mastocytosis |
|
A Jönsson, C Grännö, J Järhult & G
Roupe |
P67 |
Brown
tumour of the maxilla as the presenting feature of parathyroid
carcinoma |
|
AJ Watt, T Gruning & DEH Flanagan |
P68 |
Unexpected
detection of thyroid cancer in a patient with presumed Graves'
thyrotoxicosis |
|
AJ Watt, T Gruning & DEH Flanagan |
P69 |
Primary
hyperparathyroidism (PHPT): still a cause of hypertension resistant
to therapy |
|
AP Baptista, EC Morgado, AP Silva & PL
Neves |
P70 |
Spontaneous
pregnancy after trans-sphenoidal surgery in a patient with pituitary
hypophysitis - a case report |
|
H Siddique, V Baskar, S Dissanayeke, RN Clayton & FWF
Hanna |
P71 |
Adipsic
diabetes insipidus following pituitary surgery for a macroprolactinoma |
|
M Sherlock, A Agha, D Smith, R Crowley & C
Thompson |
P72 |
Regression
of somatotropinoma in the course of treatment with octreotide in
a female patient with acromegaly |
|
B Matuszek, M Lenart-Lipi´nska & A
Nowakowski |
P73 |
Familial
hyperparathyroidism with a mutation in the HRPT2 gene |
|
P Goulden, G Bano, VK Ajith Kumar, SV Hodgson & SS
Nussey |
P74 |
Pendred's
syndrome with three mutations |
|
P Goulden, G Bano, VK Ajith Kumar, SV Hodgson & SS
Nussey |
P75 |
About
three cases of Riedel thyroiditis |
|
MC Vantyghem, S Marcelli-Tourvieille, J Schmidt,
B Néraud, P Perimenis, E Leteurtre, C Cardot- Bauters, F
Pattou, B Carnaille & JL Wémeau |
P76 |
Parathyroid
carcinoma in a patient with chronic renal failure on long-term
dialysis |
|
MR Diaconescu, M Glod & I Costea |
P77 |
Should
prophylactic thyroidectomy be carried out in mucosal neuroma syndrome? |
|
G Spyer, S Ellard, P Turnpenny, A Hattersley & B
Vaidya |
P78 |
Synchronous
malignant para-aortic phaeochromocytoma and vagal nerve paraganglioma
in a patient with germline SDHB mutation |
|
RW McCallum, P Stanton, S Walker, V Parameswaran & T
Greenaway |
P79 |
Ophthalmic
presentations of Cushing's syndrome |
|
IM Ibrahim, A Al-Bermani & RA James |
P80 |
Long-term
outcome of untreated Cushing's syndrome due to pituitary microadenoma |
|
L Nduwayo, J Othmani & P Rousseaux |
P81 |
Invasive
prolactinoma with multiple recurrences: pituitary atypical adenoma
or pituitary carcinoma? Report of a case |
|
L Gomes, I Paiva, C Ribeiro, F Gomes, M Rito,
O Rebelo & M Carvalheiro |
P82 |
A
case of primary pigmented micronodular hyperplasia as a cause of
Cushing's syndrome |
|
A Akalin, O Son, S Isiksoy, N Kebapci & B
Efe |
P83 |
Endocrine
evaluation in a man with restrictive eating disorder |
|
M Moro, L Danesi, N Polli, E Rasi, B Filippini,
M Andrioli, M Scacchi & F Cavagnini |
P84 |
Hypopituitarism
in an adult thalassemic patient. Effects of different replacement
therapies |
|
L Danesi, A Cattaneo, E Lavezzi, M Scacchi & F
Cavagnini |
P85 |
Langerhans
cell histiocytosis; management dilemma for the adult endocrinologist! |
|
IM Ibrahim, E-L Lim, S Razvi, SHS Pearce,
N Leach, R Quinton, D Mitra, J Wilsdon, A Baborie, S Johnson, AD
Burt, K Wood, G Jones, K Windebank, J Pritchard, CO Record & SMM
Bennett |
P86 |
A
case of bacterial endocarditis in a patient with acromegaly |
|
G Bassotti, D Di Sarra, D Pietrobono, T D'Amico,
P Gargiulo & G Tamburrano |
P87 |
Gitelman's
syndrome in pregnant, type 1 diabetic patient presented with foetal
growth retardation, and bilateral hydronephrosis and hydroureter |
|
MA Elrishi, A Kilvert, B Sirnivasan & I
Lawrence |
P88 |
The
prolonged progressive course of acromegaly, complicated with diabetes
mellitus, bilateral gonarthropathy, thyroid pathology and severe
papillomatosis (clinical observation) |
|
TS Kamynina, AV Dreval & JG Pokramovich |
P89 |
A
case of adult GH deficit in a woman with autoimmune polyendocrine
syndrome type II |
|
D Pietrobono, G Bassotti, F Diacono, R Iuorio,
V Mercuri & P Gargiulo |
P90 |
Spontaneous
thrombosis of ophthalmic artery aneurysm causing isolated cortisol
deficiency |
|
A Zia, F Joseph, S Basu, TRK Varma & JP
Vora |
P91 |
Aortic
involvement in Turner syndrome |
|
M Ilyas, SL Atkin, V Mathew, C Chu & D
Ettles |
P92 |
Purely
adrenaline-secreting phaeochromocytoma: a classical presentation
of a rare entity |
|
A Merghani, KH Darzy, D Morris, R Carpenter,
A Deaner & JP Monson |
P93 |
A
scary awakening - acute paralysis in a young man |
|
LV Forrest & JK Platts |
P94 |
Systemic
amyloidosis presenting with thyrotoxicosis: a case report |
|
G Fegan, S Rasbridge & M Taylor |
P95 |
Unusual
case of pseudohypoparathyroidism type IB |
|
LCH Ciin & T Dornan |
P96 |
A
case of Cushing's syndrome and rapid course of illness |
|
J Sudagani, K Jacob, S Anwar, C Gibson, JRE
Davis & FCW Wu |
P97 |
Primary
adrenal insufficiency, gonadal failure and weak legs |
|
J Sudagani, K Jacob, S Anwar, C Gibson, JRE
Davis & FCW Wu |
P98 |
Hypocalcemic
cardiomyopathy in a patient with primary hypoparathyroidism and
Fahr's disease |
|
S Azzoug & F Chentli |
P99 |
An
unusual case of panhypopituitarism associated with positive ANCA:
atypical presentation of Wegener's disease or lymphocytic hypophysitis? |
|
F Medici & P Kelly |
P100 |
Isolated
secondary hypothyroidism in identical twins |
|
PJ Weston, AK Annamalai & S Bandyopadhyay |
P101 |
Adrenal-insufficiency
manifesting as hyperkalaemic paralysis |
|
AS Kashyap, KP Anand & S Kashyap |
P102 |
Hypercalcaemia
and hypereosinophilic syndrome in a patient with cholangiocarcinoma |
|
KP Papatheodorou, DP Papazoglou, NP Papanas,
CI Iakovidis & EM Maltezos |
P103 |
Di-George
syndrome presenting with hypocalcaemia and personality disorder
in adulthood - a case report |
|
M Jose, N Iqbal, P Gaut, D Balakrishnan & H
Maksoud |
P104 |
Phaeochromocytoma
presenting as gestational diabetes |
|
KM Evans, I Montague, BA Millward & DE
Flanagan |
P105 |
Conn's
syndrome associated with hyperprolactinaemia: two case reports.
Hypertension was cured by surgery in both cases despite a 10- and
16-year history |
|
I Talapatra, S Ghosh & DJ Tymms |
P106 |
Parathyroid
carcinoma in multiple endocrine neoplasia (MEN) type 1: two case
reports |
|
A Agha, R Carpenter, S Bhattacharya & JP
Monson |
P107 |
Co-existing
hypoparathyroidism and vitamin D deficiency causing life-threatening
hypocalcaemia |
|
L Edwards & M Abubaker |
P108 |
A
rare case of metastatic choroidal melanoma to the thyroid gland:
the importance of cytology |
|
C Vezzosi, C La Magra, P Pedaccini, M Bernardini,
S Silvestri & R Nassi |
P109 |
A
complex case of pregnancy and pegvisamont treated acromegaly |
|
AI Qureshi, G Ramanathan, A Walton, L Seal,
G Bano, I Manyonda & A Panahloo |
P110 |
Post-partum
thyroiditis (PPT): colour-Doppler ultrasonography evaluation |
|
P De Remigis, A De Remigis & L Vianale |
P111 |
The
challenges of managing metabolic derangements |
|
N Iqbal, A Gruber & G Thomson |
P112 |
Three
generations of generalised resistance to thyroid hormone (GRTH) |
|
SC McGeoch, WA Watson, E Stephen, H Watson,
A Mayo, P Abraham & JS Bevan |
P113 |
Mineral-rich
baths - an unusual source of exposure to excess iodine |
|
KD Hopkins & S Ibrahim |
P114 |
Biochemical
screening for RET negative medullary thyroid carcinoma (MTC): a
case report highlighting difficulties in the interpretation of
pentagastrin stimulated calcitonin testing |
|
DR Webb, N Seevaratnam, M Suri & P King |
P115 |
A
long-standing lump in the neck proving troublesome for the surgeons |
|
S Bandyopadhyay & JP Vora |
P116 |
A
case of isolated ACTH deficiency who developed autoimmune-mediated
hypothyroidism and hepatitis |
|
SY Kim, JH Kim & HY Bae |
P117 |
Cushing's
disease presenting as a schizophreniform psychosis |
|
RW McCallum, V Parameswaran, A Duffield,
L Hoffman, JR Burgess & T Greenaway |
P118 |
Obesity,
hypertension and elevated catecholamines |
|
AA Joshi, VKB Prabhakar, HD White, MJ Diver & JP
Vora |
P119 |
Cushing's
syndrome in an adolescent with MEN1: where is the lesion? |
|
F Smeeton, JS Davies, MF Scanlon & DA
Rees |
P120 |
Glucagonoma:
does the clinical expression depend on the presence of inherited
disease? |
|
F Smeeton, JS Davies, MF Scanlon & DA
Rees |
P121 |
A
rare cause of gynaecomastia |
|
C Ravikumar, M-F Kong, MJ Levy & TA Howlett |
P122 |
Is
the continuation of lithium treatment safe during peri-operative
periods? |
|
A Tan, S Bandyopadhyay & JP Vora |
P123 |
An
unusual cause of jaundice |
|
PJD Owen, SS Lakra, LDKE Premawardhana, A
Baghomian, A Godkin & JH Lazarus |
P124 |
Severe
thyrotoxicosis and pregnancy |
|
JH Parr, A James Jones, K Wynne & S Wahid |
P125 |
Identification
of two novel GALNT3 mutations in a patient with familial tumoral
calcinosis (FTC) |
|
AM Barbieri, M Filopanti, G Bua & P Beck-Peccoz |
P126 |
Megadenoma |
|
BCT Field, SC Barnes, MJ Wheeler, MP Powell,
SM Thomas & PV Carroll |
P127 |
Autoimmune
hypophysitis causing permanent diabetes insipidus - a case report |
|
D Grant, K Campbell & J Connell |
P128 |
Time
course of neuroendocrine dysfunction after aneurysmal subarachnoid
hemorrhage - need for reassessment even years after the hemorrhage? |
|
A Reineke, E Poll, S Levasseur, E Yagmur,
JM Gilsbach & I Kreitschmann-Andermahr |
P129 |
A
case of late onset congenital adrenal hyperplasia in a female epileptic
patient: implications for clinical practice |
|
E Davies, J Kisalu, PM Bouloux & M Thomas |
P130 |
Adult-onset
nesidioblastosis- a rare clinical case |
|
T Martins, L Gomes, J Guimarães, M
Melo & M Carvalheiro |
P131 |
Seeking
an appropriate sex of rearing in 5a-reductase deficiency |
|
S Iyer, RM Thomas & T Cheetham |
P132 |
49,XXXXY
syndrome connected with hypothyroidism |
|
B Wikiera, R Slezak, E Glab, E Barg & A
Noczynska |
P133 |
Giant
labia majora in familial partial lipodystrophy |
|
T Kyaw Tun, N Correia, NA Phelan, M Shahid,
O Buckley, W Prendeville & J Gibney |
P134 |
Pituitary
apoplexy and acromegaly: a case report |
|
K Jacob, J Sudagani, S Anwar, C Gibson, FCW
Wu, DW Ray & JRE Davis |
P135 |
The
effects of lanreotide administration vs unilateral adrenalectomy
on disease activity in GIP-dependent Cushing's syndrome |
|
M Robaczyk, B Krzyzanowska-Swiniarska, G
Kulig & K Pilarska |
P136 |
Epilepsy
at presentation of macroprolactinoma |
|
D Deepak, N Bashir, P Foy & IA MacFarlane |
P137 |
Difficulty
to distinguish hyperandrogenia due to a tumoral formation or to
polycystic ovary syndrome: a case report |
|
MP Teissier, C Combes, A Drutel & S Lopez |
P138 |
Resolution
of diagnostic uncertainties with DAX-1 gene mutation analysis |
|
P Arundel, R Fisher, C Chu & S Alvi |
P139 |
Multihormonal
disorders in 17-year-old girl with congenital hypoplastic anemia
and secondary hemochromatosis |
|
E Glab, B Wikiera & E Barg |
P140 |
Carcinoid
tumour: spontaneous regression following pregnancy |
|
EL Lim, I Macleod, D Carr, D Manas, R Quinton & A
James |
P141 |
A
rare cause of thyrotoxicosis and hypercalcemia |
|
NPN Murthy, Y Prasad, M Thomas & T Fiad |
P142 |
Maternal
virilization and female fetal pseudohermaphroditism caused by exaggerating
androgen secretion of pregnancy leutomas |
|
C Chen & Y Wang |
P143 |
Two
unusual cases of extra-adrenal phaeochromocytoma |
|
PK Singh, N Iqbal, P Strouhal, BM Singh & HN
Buch |
P144 |
Prolonged
hungry bone syndrome in a patient with Wolfram syndrome: a case
report |
|
O Basat, S Ucak, AB Oncul, S Seber, N Eren & Y
Altuntas |
P145 |
Postmenopausal
androgen excess: a clinical perspective |
|
SA Ritchie, A Collier, M McIntyre & JMC
Connell |
P146 |
Use
of pulse methylprednisolone therapy in Graves' ophthalmopathy |
|
O Nechaeva, Y Bardeeva, O Perepelova, T Shestakova & I
Chikh |
P147 |
Acute
suprarenal impairment because of an adrenal bilateral necrosis
with antiphospholipids' syndrome |
|
J Combes, S Chabroux & JP Ory |
P148 |
Challenges
in the management of an uncommon cause of diabetes insipidus |
|
K Kaushal, K Jacob & SM Shalet |
P149 |
Psychiatric
and movement disorders in primary hypoparathyroidism |
|
S Chatterjee |
P150 |
A
case report of malignant insulinoma |
|
N Jeandidier, S Boullu, L Ciarloni, S Drui,
B Louis, M Pinget, JE Kurtz & G Chabrier |
P151 |
Malignant
paraganglioma in young patient without symptoms - a case report |
|
Z Velija-Asimi |
P152 |
Secondary
amenorrhoea induced by dihydrocodeine ingestion resolves following
opiate withdrawal |
|
S González & RD Murray |
P153 |
Combined
cortisol and aldosterone hypersecretion in two unusual cases of
hypertension due to adrenocortical neoplasia |
|
SCM Miller & JMC Connell |
P154 |
Endocrine
disorders in a high secure hospital |
|
IA MacFarlane, D Deepak & GV Gill |
P155 |
Acromegaly
with a double pituitary adenoma |
|
S Chandran & C Parkinson |
P156 |
17b-Hydroxysteroid
dehydrogenase deficiency caused by homozygous H271R mutation |
|
A Bachelot, Z Chakhtoura, F Kuttenn, Y Morel & PH
Touraine |
P157 |
Small
intragenic somatic mutation associated with a germline mutation
of HRPT2 gene in a patient with sporadic primary hyperparathyroidism |
|
E Pardi, F Cetani, E Ambrogini, S Borsari,
M Lemmi, A Pinchera & C Marcocci |
P158 |
Plasma
exchange for the prevention of severe thyrotoxic exacerbation following
radioactive iodine therapy for Graves' hyperthyroidism |
|
A Wee, V DeSilva & MG Prentice |
P159 |
Not-so-silent,
silent corticotroph adenomas |
|
SGI Suliman, SE Baldeweg, O Ansorge, A Clark,
M Powell & JAH Wass |
P160 |
Cushing's
syndrome presenting with palpitations |
|
NG Lessan |
P161 |
An
unusual case of PTHrPoma with coexistent secondary hyperparathyroidism |
|
MO Sharfi, E Hardy, AA Panahloo, F Lofts & LJ
Seal |
P162 |
False
positive newborn screen for congenital hypothyroidism due to a
TSH-IgG (macro-TSH) complex |
|
DJ Halsall, SK Hall, P Barker, J Anderson,
M Fahie-Wilson, R Gama & VK Chatterjee |
P163 |
Familial
hypocalciuric hypercalcemia (FHH) caused by P748L mutation in the
calcium sensing receptor (CaSR) gene |
|
R Mahto, A Tahrani, A Macleod & RV Thakker |
P164 |
Importance
of complex evaluation of the changes in ST-segment in ECG: case
report of the patient with Addison disease and Brugada syndrome |
|
M Pura & P Vanuga |
P165 |
Metformin-associated
lactic acidosis in a Caucasian woman precipitated by acute renal
failure treated with bicarbonate haemodialysis |
|
T González Losada, L Del Olmo García,
P Martinez de Icaya, V Alcázar Lázaro, T López
del Val, M Pérez Pelayo & S Herranz Antolín |
P166 |
Dysgerminoma
and gonadoblastoma in children with complete androgen insensibility |
|
A Noczynska, T Zak & B Salmonowicz |
P167 |
Unexpected
features in Prader-Willi syndrome - case report |
|
C Vulpoi, C Rusu, MC Ungureanu, C Preda,
O Stoica & E Zbranca |
P168 |
Three
extreme cases of electrolyte imbalanceinduced seizures |
|
AG Gruber, N Iqbal & GA Thomson |
P169 |
Two
cases of idiopathic primary hypoparathyroidism |
|
C Badiu, D Cristofor & M Coculescu |
P170 |
Cushing's
syndrome due to medullary thyroid carcinoma - a case report |
|
A Sousa, E Rodrigues, A Varela, E Vinha,
D Braga, P Couto, J Lopes, M Cardoso-Oliveira & JL Medina |
P171 |
Polymyalgia
rheumatica and Hashimoto thyroiditis |
|
GN Karachalios, I Kostoglou-Athanassiou,
P Athanassiou & PH Kaldrymidis |
P172 |
Addison's
disease: soy sauce - a life-saving concoction |
|
B Bhattacharya, A Ullah, WSA Smellie, A McCulloch & AH
Heald |
P173 |
Pretibial
myxoedema: is this a marker for occult thyroid ophthalmopathy? |
|
B Bhattacharya, A Ullah, AJ McCulloch & AH
Heald |
P174 |
An
unusual carcinoid tumor in a case of Cushing syndrome |
|
ZT Turki, FA Aouididi, HS Smida, LBS Ben
Salem, RB Bouguerra & CBS Ben Slama |
