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Quoted phrase not found in phrase index: "Autosomal recessive osteopetrosis 7"
Page 1
Brain Abscess in a Patient with Osteopetrosis: A Rare Complication.
İşeri Nepesov M, Kıral E, Bozan G, Kılıç Ö, Çarman KB, Yarar C, Şaylısoy S, Dinleyici EÇ. İşeri Nepesov M, et al. J Clin Res Pediatr Endocrinol. 2021 Aug 23;13(3):358-361. doi: 10.4274/jcrpe.galenos.2020.2020.0039. Epub 2020 Aug 25. J Clin Res Pediatr Endocrinol. 2021. PMID: 32840095 Free PMC article.
Brain abscess formation is extremely rare in patients with osteopetrosis. Herein, we report a case of viridans streptococci brain abscess in an immunocompromised child diagnosed with osteopetrosis. ...
Brain abscess formation is extremely rare in patients with osteopetrosis. Herein, we report a case of viridans streptococci brain abs …
Successful hematopoietic stem cell transplantation for osteopetrosis using reduced intensity conditioning.
Shadur B, Zaidman I, NaserEddin A, Lokshin E, Hussein F, Oron HC, Avni B, Grisariu S, Stepensky P. Shadur B, et al. Pediatr Blood Cancer. 2018 Jun;65(6):e27010. doi: 10.1002/pbc.27010. Epub 2018 Feb 22. Pediatr Blood Cancer. 2018. PMID: 29469225
BACKGROUND: Infantile malignant osteopetrosis (IMO) is an autosomal recessive condition characterized by defective osteoclast activity, with hematopoietic bone marrow transplant being the only available cure. ...There were 12 cases of acute graft versus host …
BACKGROUND: Infantile malignant osteopetrosis (IMO) is an autosomal recessive condition characterized by defective oste …
Long-term outcome of haematopoietic stem cell transplantation in autosomal recessive osteopetrosis: an EBMT report.
Driessen GJ, Gerritsen EJ, Fischer A, Fasth A, Hop WC, Veys P, Porta F, Cant A, Steward CG, Vossen JM, Uckan D, Friedrich W. Driessen GJ, et al. Bone Marrow Transplant. 2003 Oct;32(7):657-63. doi: 10.1038/sj.bmt.1704194. Bone Marrow Transplant. 2003. PMID: 13130312
A retrospective analysis was made of 122 children who had received an allogeneic haematopoietic stem cell transplantation (HSCT) for autosomal recessive osteopetrosis between 1980 and 2001. The actuarial probabilities of 5 years disease free survival were 73% …
A retrospective analysis was made of 122 children who had received an allogeneic haematopoietic stem cell transplantation (HSCT) for auto …
Severe hypophosphataemia can be an early sign of osteopetrorickets: a case report.
Doulgeraki A, Bani-Odeh L, Tramma D, Giataganas G, Kirvassilis F, Kollios K, Fotoulaki M. Doulgeraki A, et al. J Pediatr Endocrinol Metab. 2023 May 5;36(7):712-715. doi: 10.1515/jpem-2023-0001. Print 2023 Jul 26. J Pediatr Endocrinol Metab. 2023. PMID: 37141118
Osteopetrorickets is a rare complication of autosomal recessive ("malignant") osteopetrosis. Its prompt diagnosis is essential, because early suspicion of infantile osteopetrosis enables treatment with human stem cell transplantation, depending on the …
Osteopetrorickets is a rare complication of autosomal recessive ("malignant") osteopetrosis. Its prompt diagnosis is es …
Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancy.
Otero JE, Gottesman GS, McAlister WH, Mumm S, Madson KL, Kiffer-Moreira T, Sheen C, Millán JL, Ericson KL, Whyte MP. Otero JE, et al. J Bone Miner Res. 2013 Feb;28(2):419-30. doi: 10.1002/jbmr.1752. J Bone Miner Res. 2013. PMID: 22972716 Free article.
Generalized arterial calcification (AC) of infancy (GACI) is an autosomal recessive disorder that features hydroxyapatite deposition within arterial elastic fibers. ...Radiographic features of osteopetrosis included osteosclerosis and femoral Erlenmeyer flask …
Generalized arterial calcification (AC) of infancy (GACI) is an autosomal recessive disorder that features hydroxyapatite depo …