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Search Results - Ghervan, C
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L’insulino-résistance sévère ? Une cause méconnue d’exophtalmie
by
Ghervan, C
,
Feier, N
,
Silaghi, A
,
Valea, A
Published in
Annales d'endocrinologie
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Quality of Life in Patients with Acromegaly - A Romanian Single Center Cross-Sectional Study
by
Scânteie, C L
,
Leucuţa, D C
,
Ghervan, C M V
Published in
Acta endocrinologica (Bucharest, Romania : 2005)
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L’incidentalome parathyroïdien – la réalité au-delà des images
by
Ghervan, C
,
Nemes, C
,
Silaghi, A
Published in
Annales d'endocrinologie
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Glycemic profile in patients with acromegaly treated with somatostatin analogue
by
Valea, A
,
Carsote, M
,
Ghervan, C
,
Georgescu, C
Published in
Journal of medicine and life
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P.3.a.014 Psychotic disorder with underlying Graves disease: a case report
by
Zaharie, A.M
,
Racataianu, N
,
Miclutia, I
,
Ghervan, C
Published in
European neuropsychopharmacology
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P1-088 - La place de l’échographie pour la localisation de la lésion dans l’hyperparathyroïdie primaire
by
Ghervan, C.
,
Ciuce, C.
,
Muntean, V.
,
Georgescu, C.
,
Valea, A.
,
Duncea, I.
Published in
Annales d'endocrinologie
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Ipogonadismo ipogonadotropo familiare isolato e mutazione del gene GNRH1
by
Bouligand, J.
,
Ghervan, C.
,
Tello, J. A.
,
Brailly-Tabard, S.
,
Salenave, S.
,
Chanson, P.
,
Lombès, M.
,
Millar, R. P.
,
Guiochon-Mantel, A.
,
Young, J.
,
Peri, Alessandro
Published in
L'Endocrinologo
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Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism
by
Badiu, Corin
,
Bonomi, Marco
,
Borshchevsky, Ivan
,
Cools, Martine
,
Craen, Margarita
,
Ghervan, Cristina
,
Hauschild, Michael
,
Hershkovitz, Eli
,
Hrabovszky, Erik
,
Juul, Anders
,
Kim, Soo-Hyun
,
Kumanov, Phillip
,
Lecumberri, Beatriz
,
Lemos, Manuel C
,
Neocleous, Vassos
,
Niedziela, Marek
,
Djurdjevic, Sandra Pekic
,
Persani, Luca
,
Phan-Hug, Franziska
,
Pignatelli, Duarte
,
Pitteloud, Nelly
,
Popovic, Vera
,
Quinton, Richard
,
Skordis, Nicos
,
Smith, Neil
,
Stefanija, Magdalena Avbelj
,
Xu, Cheng
,
Young, Jacques
,
Dwyer, Andrew A
Published in
Orphanet journal of rare diseases
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Hypogonadismes hypogonadotrophiques congénitaux et syndrome de Kallmann chez l’homme
by
Ghervan, Cristina
,
Young, Jacques
Published in
La Presse médicale (1983)
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Hypogonadismes hypogonadotrophiques congénitaux et syndrome de Kallmann chez l'homme : Fonction gonadique et reproduction masculine
by
GHERVAN, Cristina
,
YOUNG, Jacques
Published in
La Presse médicale (1983)
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The use of renal grafts with anatomical anomalies — An effective alternative to increase the living donation
by
Lucan, M.
,
Rotariu, P.
,
Ghervan, L.
,
Burghelea, C.
,
Iacob, G.
,
Elec, F.
Published in
European urology supplements : official journal of the European Association of Urology
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