Iliopsoas hematoma in a young patient with type I Gaucher disease

被引:0
作者
Jmoudiak, M
Itzchaki, M
Hadas-Halpern, I
Hrebicek, M
Hodanova, K
Elstein, D
Zimran, A
机构
[1] Shaare Zedek Med Ctr, Gaucher Clin, IL-91031 Jerusalem, Israel
[2] Shaare Zedek Med Ctr, Dept Orthoped Surg, IL-91031 Jerusalem, Israel
[3] Shaare Zedek Med Ctr, Dept Diagnost Radiol, IL-91031 Jerusalem, Israel
[4] Inst Inherited Metabol Disorders, Prague, Czech Republic
来源
ISRAEL MEDICAL ASSOCIATION JOURNAL | 2003年 / 5卷 / 09期
关键词
iliopsoas hematoma; Gaucher disease; ultrasonography;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:673 / 674
页数:2
相关论文
共 50 条
[41]   Appendiceal involvement in a patient with Gaucher disease [J].
Kocic, Marija ;
Djuricic, Slavisa M. ;
Djordjevic, Maja ;
Savic, Djordje ;
Kecman, Bozica ;
Sarajlija, Adrijan .
BLOOD CELLS MOLECULES AND DISEASES, 2018, 68 :109-111
[42]   Expansion of hematogones in a patient with Gaucher disease [J].
D'Arena, G ;
Bisceglia, M ;
Ladogana, S ;
Carella, AM ;
Carotenuto, M ;
Paolucci, P .
MEDICAL AND PEDIATRIC ONCOLOGY, 2001, 36 (06) :657-658
[43]   Enzyme replacement therapy with imiglucerase in Taiwanese patients with type I Gaucher disease [J].
Hsu, CC ;
Chien, YH ;
Lai, MY ;
Hwu, WL .
JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2002, 101 (09) :627-631
[44]   Children with type I Gaucher disease: Growing into adulthood with and without enzyme therapy [J].
Zimran, A ;
Abrahamov, A ;
Elstein, D .
ISRAEL MEDICAL ASSOCIATION JOURNAL, 2000, 2 (02) :80-81
[45]   Oxidative and chromosomal DNA damage in patients with type I Gaucher disease and carriers [J].
Uzen, Ramazan ;
Bayram, Fahri ;
Dursun, Huseyin ;
Kardas, Fatih ;
Altin-Celik, Pinar ;
Cakir, Mustafa ;
Eken, Ahmet ;
Cucer, Nurhan ;
Donmez-Altuntas, Hamiyet .
CLINICAL BIOCHEMISTRY, 2023, 111 :26-31
[46]   Clinical Characteristics and GBA Gene Mutation Analysis of Gaucher Disease Type I [J].
Zhang, Xiaofang ;
Wu, Yiping ;
Wang, Lihua ;
Wu, Qiong ;
Liu, Qian ;
Li, Ruimin .
CLINICAL LABORATORY, 2023, 69 (04) :837-839
[47]   Gaucher disease, Fabry disease and mucopolysaccharidosis type I - How can the rheumatologist recognise these patients? [J].
Manger, B ;
Mengel, E ;
Schaefer, R ;
Haase, C ;
Seidel, J ;
Michels, H .
ZEITSCHRIFT FUR RHEUMATOLOGIE, 2006, 65 (01) :32-+
[48]   Wandering spleen in a young girl with Gaucher disease [J].
Dweck, A ;
Abrahamov, A ;
Hadas-Halpern, I ;
Zimran, A ;
Elstein, D .
ISRAEL MEDICAL ASSOCIATION JOURNAL, 2001, 3 (08) :623-624
[49]   Recurrent pulmonary aspergillosis and mycobacterial infection in an unsplenectomized patient with type 1 Gaucher disease [J].
Machaczka, Maciej ;
Lorenz, Fryderyk ;
Kleinotiene, Grazina ;
Bulanda, Agnieszka ;
Markuszewska-Kuczynska, Alicja ;
Raistenskis, Juozas ;
Klimkowska, Monika .
UPSALA JOURNAL OF MEDICAL SCIENCES, 2014, 119 (01) :44-49
[50]   Patient reported outcome measures in a large cohort of patients with type 1 Gaucher disease [J].
Dinur, Tama ;
Istaiti, Majdolen ;
Frydman, Dafna ;
Becker-Cohen, Michal ;
Szer, Jeff ;
Zimran, Ari ;
Revel-Vilk, Shoshana .
ORPHANET JOURNAL OF RARE DISEASES, 2020, 15 (01)