Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 71

The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.

DIAGNOSIS OF ENDOCRINE DISEASE: Endocrine late-effects of childhood cancer and its treatments

Chemaitilly, Wassim, Cohen, Laurie E·2017·European Journal of Endocrinology

Abstract

Endocrine complications are frequently observed in childhood cancer survivors (CCS). One of two CCS will experience at least one endocrine complication during the course of his/her lifespan, most commonly as a late-effect of cancer treatments, especially radiotherapy and alkylating agent chemotherapy. Endocrine late-effects include impairments of the hypothalamus/pituitary, thyroid and gonads, as well as decreased bone mineral density and metabolic derangements leading to obesity and/or diabetes mellitus. A systematic approach where CCS are screened for endocrine late-effects based on their cancer history and treatment exposures may improve health outcomes by allowing the early diagnosis and treatment of these complications.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1530/eje-17-0054

Cites

11 of 11 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Research works printed but not linked: 194

  1. 10.3322/caac.21219 · DOI · Paper page
  2. 10.1200/JCO.2008.21.1953 · DOI · Paper page
  3. 10.1530/EJE-12-1043 · DOI
  4. Clement, 2016, Prevalence and risk factors of early endocrine disorders in childhood brain tumor survivors: a nationwide, multicenter study, Journal of Clinical Oncology, 34, 4362, 10.1200/JCO.2016.67.5025 · DOI
  5. Rose, 2004, Hypothalamic dysfunction after chemotherapy, Journal of Pediatric Endocrinology and Metabolism, 17, 55, 10.1515/JPEM.2004.17.1.55 · doi:10.1515/jpem.2004.17.1.55
  6. 10.1002/cncr.22120 · DOI · Paper page
  7. 10.1038/sj.bmt.1704481 · doi:10.1038/sj.bmt.1704481
  8. 10.1210/jc.2012-4085 · DOI
  9. Rastogi, 2012, Imatinib mesylate causes growth deceleration in pediatric patients with chronic myelogenous leukemia, Pediatric Blood and Cancer, 59, 840, 10.1002/pbc.24121 · DOI
  10. 10.1210/jc.2012-4075 · DOI · Paper page
  11. 10.1200/JCO.2008.13.5293 · DOI
  12. 10.1200/JCO.2014.56.7933 · DOI · Paper page
  13. Eaton, 2015, Endocrine outcomes with proton and photon radiotherapy for standard risk medulloblastoma, Neuro-Oncology, 18, 881, 10.1093/neuonc/nov302 · DOI
  14. Viswanathan, 2011, Pituitary hormone dysfunction after proton beam radiation therapy in children with brain tumors, Endocrine Practice, 17, 891, 10.4158/EP10391.OR · DOI
  15. Bishop, 2014, Proton beam therapy versus conformal photon radiation therapy for childhood craniopharyngioma: multi-institutional analysis of outcomes, cyst dynamics, and toxicity, International Journal of Radiation Oncology, Biology, Physics, 90, 354, 10.1016/j.ijrobp.2014.05.051 · DOI
  16. 10.1200/JCO.2016.66.6545 · DOI
  17. 10.1200/JCO.2011.37.9453 · DOI
  18. 10.1053/j.seminhematol.2013.06.007 · DOI · Paper page
  19. 10.1200/JCO.2015.64.9525 · DOI
  20. Brauner, 1986, Greater susceptibility to hypothalamopituitary irradiation in younger children with acute lymphoblastic leukemia, Journal of Pediatrics, 108, 332, 10.1016/S0022-3476(86)81027-7 · doi:10.1016/s0022-3476(86)81027-7
  21. Brauner, 1997, Contribution of growth hormone deficiency to the growth failure that follows bone marrow transplantation, Journal of Pediatrics, 130, 785, 10.1016/S0022-3476(97)80022-4 · doi:10.1016/s0022-3476(97)80022-4
  22. 10.1016/j.ecl.2007.07.002 · DOI
  23. 10.1016/S0022-3476(96)70119-1 · DOI
  24. 10.1038/sj.bmt.1705694 · DOI
  25. Couto-Silva, 2006, Final height and gonad function after total body irradiation during childhood, Bone Marrow Transplantation, 38, 427, 10.1038/sj.bmt.1705455 · DOI
  26. 10.1136/adc.66.6.689 · DOI
  27. Cohen, 1999, Final height of patients who underwent bone marrow transplantation for hematological disorders during childhood: a study by the Working Party for Late Effects-EBMT, Blood, 93, 4109
  28. Pomarede, 1984, Incidence of anterior pituitary deficiency after radiotherapy at an early age: study in retinoblastoma, Acta Paediatrica Scandinavica, 73, 115, 10.1111/j.1651-2227.1984.tb09908.x · doi:10.1111/j.1651-2227.1984.tb09908.x
  29. Friedman, 2013, Long-term medical outcomes in survivors of extra-ocular retinoblastoma: the Memorial Sloan-Kettering Cancer Center (MSKCC) experience, Pediatric Blood and Cancer, 60, 694, 10.1002/pbc.24280 · doi:10.1002/pbc.24280
  30. Cheuk, 2011, Prognostic factors and long-term outcomes of childhood nasopharyngeal carcinoma, Cancer, 117, 197, 10.1002/cncr.25376 · doi:10.1002/cncr.25376
  31. Punyko, 2005, Long-term medical effects of childhood and adolescent rhabdomyosarcoma: a report from the childhood cancer survivor study, Pediatric Blood and Cancer, 44, 643, 10.1002/pbc.20310 · DOI
  32. Clement, 2015, Endocrine disorders among long-term survivors of childhood head and neck rhabdomyosarcoma, European Journal of Cancer, 54, 1, 10.1016/j.ejca.2015.10.064 · DOI
  33. Narayanan, 2013, Growth failure in children with chronic myeloid leukemia receiving imatinib is due to disruption of GH/IGF-1 axis, Pediatric Blood and Cancer, 60, 1148, 10.1002/pbc.24397 · DOI
  34. Tauer, 2015, Impact of long-term exposure to the tyrosine kinase inhibitor imatinib on the skeleton of growing rats, PLoS ONE, 10, e0131192, 10.1371/journal.pone.0131192 · DOI
  35. 10.1210/jc.85.11.3990 · doi:10.1210/jc.85.11.3990 · Paper page
  36. Hobbie, 2011, Prevalence of advanced bone age in a cohort of patients who received cis-retinoic acid for high-risk neuroblastoma, Pediatric Blood and Cancer, 56, 474, 10.1002/pbc.22839 · DOI
  37. Clayton, 1991, The evolution of spinal growth after irradiation, Clinical Oncology, 3, 220, 10.1016/S0936-6555(05)80744-7 · DOI
  38. 10.1016/S0022-3476(76)80620-8 · DOI · Paper page
  39. 10.1210/jc.79.2.537 · DOI
  40. 10.1111/j.1365-2265.2006.02676.x · DOI
  41. 10.1016/0360-3016(94)00427-M · DOI
  42. 10.1530/acta.0.1290511 · DOI · Paper page
  43. 10.1046/j.1365-2265.1999.00804.x · DOI
  44. Grimberg, 2016, & Drug and Therapeutics Committee and Ethics Committee of the Pediatric Endocrine Society. Guidelines for growth hormone and insulin-like growth factor-I treatment in children and adolescents: growth hormone deficiency, idiopathic short stature, and primary insulin-like growth factor-I deficiency, Hormone Research in Paediatrics, 86, 361, 10.1159/000452150 · DOI · Paper page
  45. 10.1111/j.1365-2265.2005.02272.x · DOI · Paper page
  46. 10.1210/jcem-58-6-1043 · DOI
  47. 10.1002/ajpa.1330350306 · DOI
  48. 10.1210/jc.2004-0160 · DOI
  49. Ciaccio, 2010, Effectiveness of rhGH treatment on adult height in GH-deficient childhood survivors of medulloblastoma, Hormone Research in Paediatrics, 73, 281, 10.1159/000284393 · DOI
  50. 10.1530/EJE-09-0690 · doi:10.1530/eje-09-0690
  51. Chemaitilly, 2015, Central precocious puberty following the diagnosis and treatment of paediatric cancer and central nervous system tumours: presentation and long-term outcomes, Clinical Endocrinology, 84, 361, 10.1111/cen.12964 · DOI
  52. 10.1016/j.ecl.2012.07.002 · DOI
  53. 10.1210/jc.2015-1002 · DOI
  54. 10.1210/jc.2006-0656 · DOI · Paper page
  55. 10.1210/jc.87.7.3136 · DOI · Paper page
  56. 10.1210/jc.2011-0112 · DOI
  57. 10.1210/jc.2013-4159 · DOI
  58. 10.1530/EJE-11-1072 · DOI
  59. 10.1530/EJE-12-1083 · DOI
  60. 10.1046/j.1365-2265.2001.01229.x · DOI
  61. 10.1056/NEJMcp0800459 · DOI · Paper page
  62. 10.1210/jc.2015-2028 · DOI
  63. 10.1111/j.1365-2265.2006.02582.x · DOI
  64. Rossetti, 1991, Precocious puberty following BMT, Bone Marrow Transplantation, 8, 43
  65. 10.1001/archpedi.1996.02170310023003 · DOI
  66. Armstrong, 2009, Abnormal timing of menarche in survivors of central nervous system tumors: a report from the Childhood Cancer Survivor Study, Cancer, 115, 2562, 10.1002/cncr.24294 · DOI
  67. 10.1542/peds.2008-1783 · DOI · Paper page
  68. Chemaitilly, 2016, Hypothalamic-pituitary axis dysfunction in survivors of childhood CNS tumors: importance of systematic follow-up and early endocrine consultation, Journal of Clinical Oncology, 34, 4315, 10.1200/JCO.2016.70.1847 · DOI
  69. Sklar, 1990, Effects of radiation on testicular function in long-term survivors of childhood acute lymphoblastic leukemia: a report from the Children Cancer Study Group, Journal of Clinical Oncology, 8, 1981, 10.1200/JCO.1990.8.12.1981 · DOI
  70. 10.1002/1097-0142(19900315)65:6<1303::AID-CNCR2820650608>3.0.CO;2-D · doi:10.1002/1097-0142(19900315)65:6<1303::aid-cncr2820650608>3.0.co;2-d
  71. 10.1038/sj.bmt.1705612 · DOI
  72. Brignardello, 2016, Gonadal status in long-term male survivors of childhood cancer, Journal of Cancer Research and Clinical Oncology, 142, 1127, 10.1007/s00432-016-2124-5 · DOI
  73. Shalitin, 2014, Endocrine complications and components of the metabolic syndrome in survivors of childhood malignant non-brain solid tumors, Hormone Research in Paediatrics, 81, 32, 10.1159/000355577 · DOI
  74. 10.1056/NEJMcp1109290 · DOI · Paper page
  75. 10.1200/JCO.2012.43.5511 · DOI
  76. 10.1200/JCO.2011.38.6938 · DOI
  77. 10.1210/jc.84.12.4472 · doi:10.1210/jc.84.12.4472 · Paper page
  78. Follin, 2016, Long-term effect of cranial radiotherapy on pituitary-hypothalamus area in childhood acute lymphoblastic leukemia survivors, Current Treatment Options in Oncology, 17, 50, 10.1007/s11864-016-0426-0 · DOI
  79. Sanders, 1986, Growth and development following marrow transplantation for leukemia, Blood, 68, 1129, 10.1182/blood.V68.5.1129.1129 · DOI
  80. Patterson, 2009, Adrenal function testing in pediatric cancer survivors, Pediatric Blood and Cancer, 53, 1302, 10.1002/pbc.22208 · DOI
  81. Balachandar, 2014, Ovarian function in survivors of childhood medulloblastoma: impact of reduced dose craniospinal irradiation and high-dose chemotherapy with autologous stem cell rescue, Pediatric Blood and Cancer, 62, 317, 10.1002/pbc.25291 · doi:10.1002/pbc.25291
  82. 10.1210/jc.85.9.3227 · DOI · Paper page
  83. 10.1001/jama.2013.6296 · DOI · Paper page
  84. Michel, 1997, Late effects of allogeneic bone marrow transplantation for children with acute myeloblastic leukemia in first complete remission: the impact of conditioning regimen without total-body irradiation – a report from the Societe Francaise de Greffe de Moelle, Journal of Clinical Oncology, 15, 2238, 10.1200/JCO.1997.15.6.2238 · DOI
  85. Boulad, 1995, Thyroid dysfunction following bone marrow transplantation using hyperfractionated radiation, Bone Marrow Transplantation, 15, 71
  86. 10.1038/leu.2010.210 · doi:10.1038/leu.2010.210
  87. 10.1097/MD.0b013e31812f864d · DOI
  88. 10.1038/sj.bmt.1702384 · DOI
  89. van Santen, 2005, de KJ & Vulsma T. Endocrine late effects from multi-modality treatment of neuroblastoma, European Journal of Cancer, 41, 1767, 10.1016/j.ejca.2005.02.036 · DOI
  90. 10.1210/jc.2015-1690 · DOI
  91. Sklar, 2001, Endocrine complications of pediatric stem cell transplantation, Frontiers in Bioscience, 6, G17, 10.2741/A714 · doi:10.2741/a714
  92. 10.1667/RR2240.1 · DOI · Paper page
  93. 10.1158/1055-9965.EPI-11-0576 · DOI
  94. Ning, 2015, Evidence of high mortality in long term survivors of childhood medulloblastoma, Journal of Neuro-Oncology, 122, 321, 10.1007/s11060-014-1712-y · doi:10.1007/s11060-014-1712-y
  95. 10.1200/JCO.2006.08.9276 · DOI
  96. 10.1002/cncr.11362 · DOI
  97. Inamoto, 2015, Secondary solid cancer screening following hematopoietic cell transplantation, Bone Marrow Transplantation, 50, 1013, 10.1038/bmt.2015.63 · DOI
  98. Chow, 2009, Risk of thyroid dysfunction and subsequent thyroid cancer among survivors of acute lymphoblastic leukemia: a report from the Childhood Cancer Survivor Study, Pediatric Blood and Cancer, 53, 432, 10.1002/pbc.22082 · DOI
  99. 10.1046/j.1365-2265.2001.01292.x · DOI · Paper page
  100. 10.1002/(SICI)1096-8652(199809)59:1<91::AID-AJH18>3.0.CO;2-4 · doi:10.1002/(sici)1096-8652(199809)59:1<91::aid-ajh18>3.0.co;2-4
  101. Neves, 2006, Treatment for acute lymphoblastic leukemia in children is associated with papillary carcinoma of thyroid, but not with thyroid disfunction, Minerva Pediatrica, 58, 469
  102. van Santen, 2012, van der Steeg AF, Nieveen van Dijkum EJ & van Trotsenburg AS. Differentiated thyroid carcinoma after 131I-MIBG treatment for neuroblastoma during childhood: description of the first two cases, Thyroid, 22, 643, 10.1089/thy.2011.0464 · DOI
  103. Tucker, 1991, Therapeutic radiation at a young age is linked to secondary thyroid cancer. The Late Effects Study Group, Cancer Research, 51, 2885
  104. 10.1210/er.2011-0011 · DOI
  105. 10.1089/thy.2014.0460 · DOI · Paper page
  106. 10.1210/jc.2009-0337 · DOI
  107. 10.1210/jc.2006-2744 · DOI
  108. Howell, 1999, Testicular function after cytotoxic chemotherapy: evidence of Leydig cell insufficiency, Journal of Clinical Oncology, 17, 1493, 10.1200/JCO.1999.17.5.1493 · DOI
  109. 10.1136/adc.76.3.190 · doi:10.1136/adc.76.3.190
  110. 10.1210/jc.86.6.2446 · DOI
  111. 10.1016/S0022-3476(83)80584-8 · DOI
  112. Ridola, 2009, Testicular function of survivors of childhood cancer: a comparative study between ifosfamide- and cyclophosphamide-based regimens, European Journal of Cancer, 45, 814, 10.1016/j.ejca.2009.01.002 · doi:10.1016/j.ejca.2009.01.002
  113. Sanders, 2004, Endocrine complications of high-dose therapy with stem cell transplantation, Pediatric Transplantation, 8, 39, 10.1111/j.1398-2265.2004.00165.x · DOI
  114. 10.1002/(SICI)1096-911X(199905)32:5<366::AID-MPO10>3.0.CO;2-7 · doi:10.1002/(sici)1096-911x(199905)32:5<366::aid-mpo10>3.0.co;2-7
  115. Heyn, 1992, Late effects of therapy in patients with paratesticular rhabdomyosarcoma. Intergroup Rhabdomyosarcoma Study Committee, Journal of Clinical Oncology, 10, 614, 10.1200/JCO.1992.10.4.614 · doi:10.1200/jco.1992.10.4.614
  116. Giannetta, 2012, Subclinical male hypogonadism, Best Practice and Research Clinical Endocrinology and Metabolism, 26, 539, 10.1016/j.beem.2011.12.005 · DOI
  117. 10.1016/j.fertnstert.2013.08.010 · DOI · Paper page
  118. 10.1038/sj.bmt.1702695 · doi:10.1038/sj.bmt.1702695
  119. 10.1038/sj.bmt.1703651 · doi:10.1038/sj.bmt.1703651
  120. 10.1182/blood-2006-01-0176 · DOI
  121. Sanders, 1996, Pregnancies following high-dose cyclophosphamide with or without high-dose busulfan or total-body irradiation and bone marrow transplantation, Blood, 87, 3045, 10.1182/blood.V87.7.3045.bloodjournal8773045 · DOI · Paper page
  122. 10.1111/j.1365-2605.2010.01058.x · doi:10.1111/j.1365-2605.2010.01058.x
  123. 10.1016/S1470-2045(14)70408-5 · DOI · Paper page
  124. 10.1002/(SICI)1097-0142(19961101)78:9<2020::AID-CNCR25>3.0.CO;2-Y · doi:10.1002/(sici)1097-0142(19961101)78:9<2020::aid-cncr25>3.0.co;2-y
  125. Kenney, 2014, Impaired testicular function after an ifosfamide-containing regimen for pediatric osteosarcoma: a case series and review of the literature, Journal of Pediatric Hematology/Oncology, 36, 237, 10.1097/MPH.0b013e3182a27c39 · doi:10.1097/mph.0b013e3182a27c39
  126. 10.1002/1097-0142(20010201)91:3<613::AID-CNCR1042>3.0.CO;2-R · DOI
  127. Moreno, 2013, Long-term follow-up of children with high-risk neuroblastoma: the ENSG5 trial experience, Pediatric Blood and Cancer, 60, 1135, 10.1002/pbc.24452 · DOI
  128. 10.1038/sj.bmt.1705809 · doi:10.1038/sj.bmt.1705809
  129. Mariani, 2011, Severe oligozoospermia in a young man with chronic myeloid leukemia on long-term treatment with imatinib started before puberty, Fertility and Sterility, 95, e1115, 10.1016/j.fertnstert.2010.08.060 · DOI
  130. 10.1056/NEJM200411113512024 · DOI
  131. 10.1016/j.leukres.2014.09.016 · DOI · Paper page
  132. 10.1080/088800100276631 · doi:10.1080/088800100276631
  133. Anderson, 2015, Cancer treatment and gonadal function: experimental and established strategies for fertility preservation in children and young adults, Lancet Diabetes and Endocrinology, 3, 556, 10.1016/S2213-8587(15)00039-X · DOI · Paper page
  134. 10.1200/JCO.2015.64.3288 · DOI
  135. 10.1210/jc.2006-0020 · DOI · Paper page
  136. 10.1136/adc.63.5.495 · DOI
  137. 10.1093/jnci/djj243 · DOI · Paper page
  138. Frisk, 2004, Pubertal development and final height after autologous bone marrow transplantation for acute lymphoblastic leukemia., Bone Marrow Transplantation, 33, 205, 10.1038/sj.bmt.1704324 · DOI
  139. Madden, 2016, Long-term follow-up after reduced-intensity conditioning and stem cell transplantation for childhood nonmalignant disorders, Biology of Blood and Marrow Transplantation, 22, 1467, 10.1016/j.bbmt.2016.04.025 · doi:10.1016/j.bbmt.2016.04.025
  140. Matsumoto, 1999, Ovarian function after bone marrow transplantation performed before menarche, Archives of Disease in Childhood, 80, 452, 10.1136/adc.80.5.452 · DOI
  141. 10.1016/S0022-3476(97)70345-7 · DOI
  142. Sanders, 1988, Ovarian function following marrow transplantation for aplastic anemia or leukemia, Journal of Clinical Oncology, 6, 813, 10.1200/JCO.1988.6.5.813 · doi:10.1200/jco.1988.6.5.813
  143. 10.1038/sj.bmt.1701569 · doi:10.1038/sj.bmt.1701569
  144. 10.1111/j.1471-0528.1999.tb08180.x · DOI
  145. 10.1002/mpo.2950210505 · DOI
  146. Freycon, 2015, Age at birth of first child and fecundity of women survivors of childhood acute lymphoblastic leukemia (1987–2007): a study of the childhood cancer registry of the Rhone-Alpes Region in France (ARCERRA), Pediatric Hematology and Oncology, 32, 273, 10.3109/08880018.2015.1020178 · doi:10.3109/08880018.2015.1020178
  147. 10.1093/humupd/dmr038 · DOI
  148. Hamre, 2012, Gonadal function and parenthood 20 years after treatment for childhood lymphoma: a cross-sectional study, Pediatric Blood and Cancer, 59, 271, 10.1002/pbc.23363 · DOI
  149. 10.1002/(SICI)1096-911X(199910)33:4<362::AID-MPO4>3.0.CO;2-I · doi:10.1002/(sici)1096-911x(199910)33:4<362::aid-mpo4>3.0.co;2-i
  150. 10.3109/08880010903019344 · DOI
  151. Oue, 2015, Problems during the long-term follow-up after surgery for pediatric solid malignancies, European Journal of Pediatric Surgery, 25, 123
  152. Clement, 2014, Primary ovarian insufficiency in children after treatment with 131I-metaiodobenzylguanidine for neuroblastoma: report of the first two cases, Journal of Clinical Endocrinology and Metabolism, 99, E112, 10.1210/jc.2013-3595 · DOI · Paper page
  153. 10.1016/j.fertnstert.2012.09.028 · DOI · Paper page
  154. Jacobson, 2016, Menses resumption after cancer treatment-induced amenorrhea occurs early or not at all, Fertility and Sterility, 105, 765, 10.1016/j.fertnstert.2015.11.020 · DOI
  155. Mostoufi-Moab, 2014, Bone morbidity in childhood leukemia: epidemiology, mechanisms, diagnosis, and treatment, Current Osteoporosis Reports, 12, 300, 10.1007/s11914-014-0222-3 · doi:10.1007/s11914-014-0222-3
  156. 10.1210/jc.2012-2393 · DOI
  157. 10.1542/peds.2007-1396 · DOI
  158. Gurney, 2014, Bone mineral density among long-term survivors of childhood acute lymphoblastic leukemia: results from the St. Jude Lifetime Cohort Study, Pediatric Blood and Cancer, 61, 1270, 10.1002/pbc.25010 · DOI
  159. 10.1210/jc.2005-1927 · DOI
  160. 10.1038/sj.bmt.1704360 · doi:10.1038/sj.bmt.1704360
  161. Dvorak, 2011, NCI, NHLBI/PBMTC first international conference on late effects after pediatric hematopoietic cell transplantation: endocrine challenges-thyroid dysfunction, growth impairment, bone health, & reproductive risks, Biology of Blood and Marrow Transplantation, 17, 1725, 10.1016/j.bbmt.2011.10.006 · DOI
  162. 10.1038/sj.bmt.1701275 · DOI
  163. 10.1002/jbmr.1499 · DOI
  164. Aisenberg, 1998, Bone mineral density in young adult survivors of childhood cancer, Journal of Pediatric Hematology/Oncology, 20, 241, 10.1097/00043426-199805000-00010 · DOI
  165. 10.1038/sj.bmt.1702131 · DOI
  166. 10.1038/sj.bmt.1703149 · DOI
  167. 10.1038/sj.bmt.1704618 · DOI
  168. 10.1016/S0022-3476(05)80536-0 · DOI
  169. Petryk, 2014, Bone mineral deficits in recipients of hematopoietic cell transplantation: the impact of young age at transplant, Bone Marrow Transplantation, 49, 258, 10.1038/bmt.2013.156 · DOI
  170. Cohen, 2012, Bone density in post-pubertal adolescent survivors of childhood brain tumors, Pediatric Blood and Cancer, 58, 959, 10.1002/pbc.23300 · DOI
  171. 10.1002/cncr.11095 · DOI · Paper page
  172. 10.1002/cncr.22546 · DOI
  173. 10.1210/jc.2002-021180 · DOI · Paper page
  174. 10.1210/er.2013-1115 · DOI · Paper page
  175. 10.1542/peds.2013-3332 · DOI · Paper page
  176. 10.1200/JCO.2008.16.3527 · DOI · Paper page
  177. Zhang, 2014, Predictors of being overweight or obese in survivors of pediatric acute lymphoblastic leukemia (ALL), Pediatric Blood and Cancer, 61, 1263, 10.1002/pbc.24960 · doi:10.1002/pbc.24960
  178. Armenian, 2017, National institutes of health hematopoietic cell transplantation late effects initiative: the cardiovascular disease and associated risk factors working group report, Biology of Blood and Marrow Transplantation, 23, 201, 10.1016/j.bbmt.2016.08.019 · DOI
  179. Hoffmeister, 2004, Diabetes mellitus in long-term survivors of pediatric hematopoietic cell transplantation, Journal of Pediatric Hematology/Oncology, 26, 81, 10.1097/00043426-200402000-00003 · DOI
  180. 10.1016/S0140-6736(00)02717-3 · DOI · Paper page
  181. Chow, 2013, Differential effects of radiotherapy on growth and endocrine function among acute leukemia survivors: a childhood cancer survivor study report, Pediatric Blood and Cancer, 60, 110, 10.1002/pbc.24198 · DOI
  182. 10.1210/jc.2006-0128 · DOI
  183. Wei, 2015, Reduced beta-cell reserve and pancreatic volume in survivors of childhood acute lymphoblastic leukaemia treated with bone marrow transplantation and total body irradiation, Clinical Endocrinology, 82, 59, 10.1111/cen.12575 · DOI
  184. Wei, 2015, Reduced insulin sensitivity in childhood survivors of haematopoietic stem cell transplantation is associated with lipodystropic and sarcopenic phenotypes, Pediatric Blood and Cancer, 62, 1992, 10.1002/pbc.25601 · DOI
  185. 10.1038/bmt.2013.218 · DOI
  186. 10.1001/archinternmed.2009.209 · DOI · Paper page
  187. 10.1371/journal.pone.0052237 · DOI
  188. 10.1016/S1470-2045(12)70323-6 · DOI
  189. 10.1038/bmt.2011.118 · DOI
  190. 10.1210/jc.2002-030003 · DOI · Paper page
  191. Hamilton, 2011, Hypothalamic obesity following craniopharyngioma surgery: results of a pilot trial of combined diazoxide and metformin therapy, International Journal of Pediatric Endocrinology, 2011, 417949, 10.1155/2011/417949 · DOI · Paper page
  192. Mason, 2002, The use of dextroamphetamine to treat obesity and hyperphagia in children treated for craniopharyngioma, Archives of Pediatrics and Adolescent Medicine, 156, 887, 10.1001/archpedi.156.9.887 · DOI · Paper page
  193. Lomenick, 2016, A 52-week pilot study of the effects of exenatide on body weight in patients with hypothalamic obesity, Obesity, 24, 1222, 10.1002/oby.21493 · DOI
  194. Cohen, 2016, Update on childhood craniopharyngiomas, Current Opinion in Endocrinology, Diabetes and Obesity, 23, 339, 10.1097/MED.0000000000000264 · DOI

Cited by

See all 71

Metadata

Authors
Chemaitilly, W., & Cohen, L. E.
Affiliations
  • 1Departments of Pediatric Medicine-Division of Endocrinology
  • 2Departments of Epidemiology and Cancer ControlSt Jude Children’s Research Hospital, Memphis, Tennessee, USA
Venue
European Journal of Endocrinology
Published
2017-04
Volume
176
Issue
4
Pages
R183-R203
ISSN
  • 0804-4643
  • 1479-683X
Cited by
71
References
11

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.