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Search Results - Appelman-Dijkstra, NM
Search Results - Appelman-Dijkstra, NM
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Paget's disease of bone
by
Appelman-Dijkstra, Natasha M.
,
Papapoulos, Socrates E.
Published in
Baillière's best practice & research. Clinical endocrinology & metabolism
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Outcome of Long‐Term Bisphosphonate Therapy in McCune‐Albright Syndrome and Polyostotic Fibrous Dysplasia
by
Majoor, Bas CJ
,
Appelman‐Dijkstra, Natasha M
,
Fiocco, Martha
,
van de Sande, Michiel AJ
,
Dijkstra, PD Sander
,
Hamdy, Neveen AT
Published in
Journal of bone and mineral research
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Clinical and translational pharmacological aspects of the management of fibrous dysplasia of bone
by
Rotman, Marlous
,
Hamdy, Neveen Agnes Therese
,
Appelman‐Dijkstra, Natasha M.
Published in
British journal of clinical pharmacology
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European expert consensus on practical management of specific aspects of parathyroid disorders in adults and in pregnancy: recommendations of the ESE Educational Program of Parathy...
by
Bollerslev, Jens
,
Rejnmark, Lars
,
Zahn, Alexandra
,
Heck, Ansgar
,
Appelman-Dijkstra, Natasha M
,
Cardoso, Luis
,
Hannan, Fadil M
,
Cetani, Filomena
,
Sikjaer, Tanja
,
Formenti, Anna Maria
,
Björnsdottir, Sigridur
,
Schalin-Jäntti, Camilla
,
Belaya, Zhanna
,
Gibb, Fraser
,
Lapauw, Bruno
,
Amrein, Karin
,
Wicke, Corinna
,
Grasemann, Corinna
,
Krebs, Michael
,
Ryhänen, Eeva
,
Makay, Özer
,
Minisola, Salvatore
,
Gaujoux, Sébastien
,
Bertocchio, Jean-Philippe
,
Hassan-Smith, Zaki
,
Linglart, Agnès
,
Winter, Elizabeth M
,
Kollmann, Martina
,
Zmierczak, Hans-Georg
,
Tsourdi, Elena
,
Pilz, Stefan
,
Siggelkow, Heide
,
Gittoes, Neil
,
Marcocci, Claudio
,
Kamenický, Peter
Published in
European journal of endocrinology
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Real-world evidence in achondroplasia: considerations for a standardized data set
by
Alanay, Yasemin
,
Mohnike, Klaus
,
Nilsson, Ola
,
Alves, Inês
,
AlSayed, Moeenaldeen
,
Appelman-Dijkstra, Natasha M
,
Baujat, Genevieve
,
Ben-Omran, Tawfeg
,
Breyer, Sandra
,
Cormier-Daire, Valerie
,
Gregersen, Pernille Axél
,
Guillén-Navarro, Encarna
,
Högler, Wolfgang
,
Maghnie, Mohamad
,
Mukherjee, Swati
,
Cohen, Shelda
,
Pimenta, Jeanne
,
Selicorni, Angelo
,
Semler, J Oliver
,
Sigaudy, Sabine
,
Popkov, Dmitry
,
Sabir, Ian
,
Noval, Susana
,
Sessa, Marco
,
Irving, Melita
Published in
Orphanet journal of rare diseases
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The Polygenic and Monogenic Basis of Paediatric Fractures
by
Ghatan, S.
,
Costantini, A.
,
Li, R.
,
De Bruin, C.
,
Appelman-Dijkstra, N. M.
,
Winter, E. M.
,
Oei, L.
,
Medina-Gomez, Carolina
Published in
Current osteoporosis reports
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Outcome of COVID-19 infections in patients with adrenal insufficiency and excess
by
Nowotny, Hanna F.
,
Bryce, Jillian
,
Ali, Salma R
,
Giordano, Roberta
,
Baronio, Federico
,
Chifu, Irina
,
Tschaidse, Lea
,
Cools, Martine
,
Van den Akker, Erica L T
,
Falhammar, Henrik
,
Appelman-Dijkstra, Natasha M.
,
Persani, Luca
,
Beccuti, Guglielmo
,
Ross, Ian L
,
Grozinsky-Glasberg, Simona
,
Pereira, Alberto M
,
Husebye, Eystein S
,
Hahner, Stephanie
,
Ahmed, S. Faisal
,
Reisch, Nicole
Published in
Endocrine Connections
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Venous thromboembolism in Cushing syndrome: results from an EuRRECa and Endo-ERN survey
by
Cherenko, M
,
Appelman-Dijkstra, N M
,
Priego Zurita, A L
,
Biermasz, N R
,
Dekkers, O M
,
Klok, F A
,
Reisch, N
,
Aulinas, A
,
Biagetti, B
,
Cannavo, S
,
Canu, L
,
Detomas, M
,
Devuyst, F
,
Falhammar, H
,
Feelders, R A
,
Ferrau, F
,
Gatto, F
,
Grasselli, C
,
van Houten, P
,
Hoybye, C
,
Isidori, A M
,
Kyrilli, A
,
Loli, P
,
Maiter, D
,
Nowak, E
,
Pivonello, R
,
Ragnarsson, O
,
Steenaard, R V
,
Unger, N
,
van de Ven, A
,
Webb, S M
,
Yeste, D
,
Ahmed, S F
,
Pereira, A M
Published in
Endocrine Connections
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Electronic reporting of rare endocrine conditions within a clinical network: results from the EuRRECa project
by
Ali, S R
,
Bryce, J
,
Priego-Zurita, A L
,
Cherenko, M
,
Smythe, C
,
de Rooij, T M
,
Cools, M
,
Danne, T
,
Katugampola, H
,
Dekkers, O M
,
Hiort, O
,
Linglart, A
,
Netchine, I
,
Nordenstrom, A
,
Attila, P
,
Persani, L
,
Reisch, N
,
Smyth, A
,
Sumnik, Z
,
Taruscio, D
,
Visser, W E
,
Pereira, A M
,
Appelman-Dijkstra, N M
,
Ahmed, S F
Published in
Endocrine Connections
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Loss-of-function mutations in the immunoglobulin superfamily member 1 gene ( IGSF1 ) cause a novel, X-linked syndrome of central hypothyroidism and testicular enlargement
by
Schoenmakers, N, Dr
,
Sun, Y
,
Bak, B
,
van Trotsenburg, ASP
,
Oostdijk, W
,
Voshol, P
,
Cambridge, E
,
White, JK
,
le Tissier, P
,
Gharavy, SNM
,
Martinez-Barbera, JP
,
Stokvis-Brantsma, WH
,
Vulsma, T
,
Kempers, MJ
,
Persani, L
,
Campi, I
,
Bonomi, M
,
Beck-Peccoz, P
,
Zhu, H
,
Davis, TME
,
Hokken-Koelega, ACS
,
Del Blanco, D Gorbenko
,
Rangasami, JJ
,
Ruivenkamp, CAL
,
Laros, JFJ
,
Kriek, M
,
Kant, SG
,
Bosch, CAJ
,
Biermasz, NR
,
Appelman-Dijkstra, NM
,
Corssmit, EP
,
Hovens, GCJ
,
Pereira, AM
,
den Dunnen, JT
,
Wade, MG
,
Breuning, MH
,
Hennekam, RC
,
Dattani, MT
,
Wit, JM
,
Bernard, DJ
,
Chatterjee, K
Published in
The Lancet (British edition)
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