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[Hypoparathyroidism and early onset dementia: Fahr syndrome should be suspected].

Kechaou I, Boukhris I.

Pan Afr Med J. 2018 May 29;30:82. doi: 10.11604/pamj.2018.30.82.15587. eCollection 2018. French.


Self-report of psychological symptoms in hypoparathyroidism patients on conventional therapy.

Arneiro AJ, Duarte BCC, Kulchetscki RM, Cury VBS, Lopes MP, Kliemann BS, Bini IB, Assad M, Biagini GLK, Borba VZC, Moreira CA.

Arch Endocrinol Metab. 2018 Jun;62(3):319-324. doi: 10.20945/2359-3997000000041. Epub 2018 May 17.


Diagnosis and treatment of hypoparathyroidism: a position statement from the Brazilian Society of Endocrinology and Metabolism.

Maeda SS, Moreira CA, Borba VZC, Bandeira F, Farias MLF, Borges JLC, Paula FJA, Vanderlei FAB, Montenegro FLM, Santos RO, Ferraz-de-Souza B, Lazaretti-Castro M.

Arch Endocrinol Metab. 2018 Feb;62(1):106-124. doi: 10.20945/2359-3997000000015.


Iatrogenic hypoparathyroidism after surgery for retrosternal goitre. A single centre retrospective analysis.

Damiano G, Cocchiara G, Palumbo VD, Fatica F, Caternicchia F, Lo Monte AI, Cajozzo M.

Clin Ter. 2018 Mar-Apr;169(2):e67-e70. doi: 10.7417/T.2018.2056.


Misdiagnosis of idiopathic hypoparathyroidism: A case report and literature review.

Li L, Yang H, Li J, Yu Y, Wang F, Zhu X, Liu G.

Medicine (Baltimore). 2018 Mar;97(9):e9884. doi: 10.1097/MD.0000000000009884. Review.


Milk-alkali syndrome (MAS) as a complication of the treatment of hypoparathyroidism - a case study.

Skwarek A, Pachucki J, Bednarczuk T, Żurecka Z, Popow M, Kondracka A, Bartoszewicz Z.

Endokrynol Pol. 2018;69(2):200-204. doi: 10.5603/EP.a2018.0015. Epub 2018 Feb 14.


The impact of different surgical procedures on hypoparathyroidism after thyroidectomy: A population-based study.

Chen KC, Iqbal U, Nguyen PA, Hsu CH, Huang CL, Hsu YE, Atique S, Islam MM, Li YJ, Jian WS.

Medicine (Baltimore). 2017 Oct;96(43):e8245. doi: 10.1097/MD.0000000000008245.


Rare case of massive pericardial effusion secondary to primary hypoparathyroidism.

Khanal S, Sharma R, Budakoty S.

Indian Heart J. 2017 Sep - Oct;69(5):660-661. doi: 10.1016/j.ihj.2017.08.026. Epub 2017 Aug 31. No abstract available.


Risk factors of hypoparathyroidism following total thyroidectomy with central lymph node dissection.

Su A, Wang B, Gong Y, Gong R, Li Z, Zhu J.

Medicine (Baltimore). 2017 Sep;96(39):e8162. doi: 10.1097/MD.0000000000008162.


Safety and Efficacy of Recombinant Human Parathyroid Hormone in Adults With Hypoparathyroidism Randomly Assigned to Receive Fixed 25-μg or 50-μg Daily Doses.

Bilezikian JP, Clarke BL, Mannstadt M, Rothman J, Vokes T, Lee HM, Krasner A.

Clin Ther. 2017 Oct;39(10):2096-2102. doi: 10.1016/j.clinthera.2017.08.011. Epub 2017 Sep 21.


Continuous Subcutaneous Recombinant Parathyroid Hormone (1-34) Infusion in the Management of Childhood Hypoparathyroidism Associated with Malabsorption.

Saraff V, Rothenbuhler A, Högler W, Linglart A.

Horm Res Paediatr. 2018;89(4):271-277. doi: 10.1159/000479867. Epub 2017 Sep 19.


[Risk factors' analysis of transient and permanent hypoparathyroidism after thyroidectomy].

Cocchiara G, Cajozzo M, Fazzotta S, Palumbo VD, Geraci G, Maione C, Buscemi S, Romano G, Fatica F, Spinelli G, Ficarella S, Maffongelli A, Caternicchia F, Lo Monte AI.

Clin Ter. 2017 Jul-Aug;168(4):e271-e277. doi: 10.7417/T.2017.2019. Review. Italian.


Unusual Proliferative Glomerulonephritis in a Patient Diagnosed to Have Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia (HDR) Syndrome with a Novel Mutation in the GATA3 Gene.

Kamezaki M, Kusaba T, Adachi T, Yamashita N, Nakata M, Ota N, Shiotsu Y, Ishida M, Usui T, Tamagaki K.

Intern Med. 2017;56(11):1393-1397. doi: 10.2169/internalmedicine.56.7930. Epub 2017 Jun 1.


A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome.

Chu XY, Li YP, Nie M, Wang O, Jiang Y, Li M, Xia WB, Xing XP.

Chin Med J (Engl). 2017 Jun 5;130(11):1378-1380. doi: 10.4103/0366-6999.206348. No abstract available.


Treatment of severe hypocalcaemia due to osteoblastic metastases in a patient with post-thyroidectomy hypoparathyroidism with 153Sm-EDTMP.

Kassi E, Kapsali I, Kokkinos M, Gogas H.

BMJ Case Rep. 2017 May 16;2017. pii: bcr-2017-219354. doi: 10.1136/bcr-2017-219354.


[Fahr syndrome secondary to primary hypoparathyroidism: about a case].

El Boukhrissi F, Zoulati G, En-Nafaa I, Ouleghzal H, Derrou S, Safi S, Bamou Y, Balouch L.

Pan Afr Med J. 2017 Jan 4;26:2. doi: 10.11604/pamj.2017.26.2.10689. eCollection 2017. French.


A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism.

Pillar N, Pleniceanu O, Fang M, Ziv L, Lahav E, Botchan S, Cheng L, Dekel B, Shomron N.

Hum Genet. 2017 Jul;136(7):835-845. doi: 10.1007/s00439-017-1804-9. Epub 2017 Apr 25.


Idiopathic hypoparathyroidism with extensive intracranial calcification in children: First report from Saudi Arabia.

Kamal NM, Alghamdi HA, Halabi AA, Bakkar AA, Algarni A, Alharbi A, Alharthi AA, Alharbi RA, Sherief LM.

Medicine (Baltimore). 2017 Apr;96(16):e6347. doi: 10.1097/MD.0000000000006347.


Exome Sequencing Reveals Mutations in AIRE as a Cause of Isolated Hypoparathyroidism.

Li D, Streeten EA, Chan A, Lwin W, Tian L, Pellegrino da Silva R, Kim CE, Anderson MS, Hakonarson H, Levine MA.

J Clin Endocrinol Metab. 2017 May 1;102(5):1726-1733. doi: 10.1210/jc.2016-3836.


Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome.

Wang L, Lin QF, Wang HY, Guan J, Lan L, Xie LY, Yu L, Yang J, Zhao C, Liang JL, Zhou HL, Yang HM, Xiong WP, Zhang QJ, Wang DY, Wang QJ.

Chin Med J (Engl). 2017 Mar 20;130(6):703-709. doi: 10.4103/0366-6999.201600.

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