Works matching DE "HEREDITARY spherocytosis"

Results: 72

The effect of preanalytical phase on the stability of osmotic fragility and morphological changes in bovine (Bos taurus) erythrocytes in cattle.

Published in:

Animal Science & Genetics, 2024, v. 20, n. 1, p. 43, doi. 10.5604/01.3001.0054.4653

By:

Adam Antos, Piotr;
Machura, Marta

Publication type:

Article

Spinal Cord Infarction in a Patient with Hereditary Spherocytosis: A Case Report and Discussion.

Published in:

Case Reports in Neurological Medicine, 2016, p. 1, doi. 10.1155/2016/7024120

By:

Waheed, Waqar;
Varigonda, Anjali L.;
Holmes, Chris E.;
Trevino, Christopher;
Borden, Neil M.;
Pendlebury, W.

Publication type:

Article

Management of hereditary angioedema in pregnant women: a review.

Published in:

International Journal of Women's Health, 2014, v. 6, p. 839, doi. 10.2147/IJWH.S46460

By:

Caballero, Teresa;
Canabal, Julio;
Rivero-Paparoni, Daniela;
Cabañas, Rosario

Publication type:

Article

Human parvovirus B19-induced aplastic crisis in an adult patient with hereditary spherocytosis: a case report and review of the literature.

Published in:

2014

By:

Yujin Kobayashi;
Yoshihiro Hatta;
Yusaku Ishiwatari;
Hitoshi Kanno;
Masami Takei

Publication type:

Case Study

First experience with single incision laparoscopic surgery in Slovakia: Concomitant cholecystectomy and splenectomy in an 11-year-old girl with hereditary spherocytosis.

Published in:

Biomedical Papers of the Medical Faculty of Palacky University in Olomouc, 2014, v. 158, n. 3, p. 479, doi. 10.5507/bp.2013.058

By:

Cingel, Vladimir;
Zabojnikova, Lenka;
Kurucova, Patricia;
Varga, Ivan

Publication type:

Article

Comparison Study of the Eosin-5'-Maleimide Binding Test, Flow Cytometric Osmotic Fragility Test, and Cryohemolysis Test in the Diagnosis of Hereditary Spherocytosis.

Published in:

American Journal of Clinical Pathology, 2014, v. 142, n. 4, p. 474, doi. 10.1309/AJCPO7V4OGXLIIPP

By:

Sang Hyuk Park;
Chan-Jeoung Park;
Bo-Ra Lee;
Young-Uk Cho;
Seongsoo Jang;
Nayoung Kim;
Kyung-Nam Koh;
Ho-Joon Im;
Jong-Jin Seo;
Eun Sil Park;
Ji Won Lee;
Keon Hee Yoo;
Hye Lim Jung

Publication type:

Article

Gallbladder Disease in Children: A 20-year Single-center Experience.

Published in:

Indian Pediatrics, 2019, v. 56, n. 5, p. 384, doi. 10.1007/s13312-019-1535-1

By:

Pogorelic, Zenon;
Aralica, Maja;
Jukic, Miro;
Zitko, Vanda;
Despot, Ranka;
Juric, Ivo

Publication type:

Article

Growth failure in hereditary spherocytosis and the effect of splenectomy.

Published in:

Indian Pediatrics, 2017, v. 54, n. 7, p. 563, doi. 10.1007/s13312-017-1069-3

By:

Das, Anirban;
Bansal, Deepak;
Trehan, Amita;
Das, Reena

Publication type:

Article

Membrane Protein Detection and Morphological Analysis of Red Blood Cells in Hereditary Spherocytosis by Confocal Laser Scanning Microscopy.

Published in:

Microscopy & Microanalysis, 2023, v. 29, n. 2, p. 777, doi. 10.1093/micmic/ozac055

By:

Rey-Barroso, Laura;
Roldán, Mónica;
Burgos-Fernández, Francisco J;
Isola, Ignacio;
Llobet, Anna Ruiz;
Gassiot, Susanna;
Sarrate, Edurne;
Vilaseca, Meritxell

Publication type:

Article

Pulmonary arterial hypertension associated with hereditary spherocytosis and splenectomy in a patient with a mutation in the BMPR2 gene.

Published in:

Clinical Case Reports, 2016, v. 4, n. 8, p. 752, doi. 10.1002/ccr3.610

By:

Baloira, Adolfo;
Bastos, María;
Pousada, Guillermo;
Valverde, Diana

Publication type:

Article

Subtotal Splenectomy in Hereditary Spherocytosis - Advantages and Disadvantages.

Published in:

Current Health Sciences Journal, 2016, v. 42, n. 4, p. 408, doi. 10.12865/CHSJ.42.04.11

By:

BICĂ, CĂTĂLINA;
CISMARU, LIANA;
STĂNESCU, LIGIA;
BICĂ, M.;
MARINESCU, DANIELA

Publication type:

Article

Particularităţi de management al unui caz de purpură trombocitopenică imună supraacută în sarcină, finalizat cu splenectomie.

Published in:

Romanian Journal of Medical Practice, 2015, v. 10, n. 1, p. 73, doi. 10.37897/rjmp.2015.1.12

By:

NICA, Adriana;
VLĂDĂREANU, Ana Maria;
ONISÂI, Minodora;
DUMITRU, Ion;
MARINESCU, Cristina;
MIHAI, Felicia;
ANCA, Florin;
VASILE, Dănuţ;
PETRE, Raluca;
BIRJARU, Andreea;
COPACIU, Elena

Publication type:

Article

Comparison and evaluation of three screening tests of hereditary spherocytosis in Chinese patients.

Published in:

Annals of Hematology, 2015, v. 94, n. 5, p. 747, doi. 10.1007/s00277-014-2270-2

By:

Tao, Yi-feng;
Deng, Zeng-fu;
Liao, Lin;
Qiu, Yu-ling;
Chen, Wen-qiang;
Lin, Fa-quan

Publication type:

Article

Automated reticulocyte parameters for hereditary spherocytosis screening.

Published in:

Annals of Hematology, 2014, v. 93, n. 11, p. 1809, doi. 10.1007/s00277-014-2127-8

By:

Lazarova, Elena;
Pradier, Olivier;
Cotton, Frédéric;
Gulbis, Béatrice

Publication type:

Article

Two different pathogenic gene mutations coexisted in the same hereditary spherocytosis family manifested with heterogeneous phenotypes.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0826-7

By:

Shen, Hongwei;
Huang, Hui;
Luo, Kaizhong;
Yi, Yan;
Shi, Xiaoliu

Publication type:

Article

SPLENECTOMY FOR HAEMATOLOGICAL DISORDERS.

Published in:

Contributions / Prilozi (1857-9345), 2014, v. 35, n. 1, p. 181

By:

Jankulovski, Nikola;
Antovic, Svetozar;
Kuzmanovska, Biljana;
Mitevski, Aleksandar

Publication type:

Article

Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis.

Published in:

2016

By:

Yuichi Matsuzaki;
Hideyuki Tomioka;
Masaki Saso;
Takashi Azuma;
Satoshi Saito;
Shigeyuki Aomi;
Kenji Yamazaki;
Matsuzaki, Yuichi;
Tomioka, Hideyuki;
Saso, Masaki;
Azuma, Takashi;
Saito, Satoshi;
Aomi, Shigeyuki;
Yamazaki, Kenji

Publication type:

journal article

Hereditary spherocytosis in a patient undergoing coronary artery bypass grafting with cardiopulmonary bypass – a case report.

Published in:

Perfusion, 2015, v. 30, n. 1, p. 77, doi. 10.1177/0267659114529323

By:

Spegar, J;
Riha, H;
Kotulak, T;
Vanek, T

Publication type:

Article

Iron oxides in human spleen.

Published in:

BioMetals, 2015, v. 28, n. 5, p. 913, doi. 10.1007/s10534-015-9876-2

By:

Kopáni, Martin;
Miglierini, Marcel;
Lančok, Adriana;
Dekan, Július;
Čaplovicová, Mária;
Jakubovský, Ján;
Boča, Roman;
Mrazova, Hedviga

Publication type:

Article

Tuning of Differential Lipid Order Between Submicrometric Domains and Surrounding Membrane Upon Erythrocyte Reshaping.

Published in:

Cellular Physiology & Biochemistry (Karger AG), 2018, v. 48, n. 6, p. 2563, doi. 10.1159/000492700

By:

Leonard, Catherine;
Pollet, Hélène;
Vermylen, Christiane;
Gov, Nir;
Tyteca, Donatienne;
Mingeot-Leclercq, Marie-Paule

Publication type:

Article

Clinical and genetic diagnosis of two Turkish patients with hereditary spherocytosis.

Published in:

European Research Journal, 2025, v. 11, n. 1, p. 129, doi. 10.18621/eurj.1512399

By:

Coşkun, Çağrı

Publication type:

Article

α-thalassaemia combined with hereditary spherocytosis in the same patient.

Published in:

Experimental & Therapeutic Medicine, 2018, v. 15, n. 2, p. 1298, doi. 10.3892/etm.2017.5579

By:

Li, Xiaohong;
Liao, Lin;
Deng, Xuelian;
Huang, Jian;
Deng, Zengfu;
Wei, Hongying;
Mo, Wuning;
Lin, Faquan

Publication type:

Article

Disorders of the erythrocyte membrane.

Published in:

Italian Journal of Medicine, 2015, v. 9, n. 4, p. 323, doi. 10.4081/itjm.2015.470

By:

Delicou, Sophia;
Xydaki, Aikaterini;
Kontaxi, Chryssanthi;
Maragkos, Konstantinos

Publication type:

Article

Previously undiagnosed hereditary spherocytosis in a patient with jaundice and pyelonephritis: a case report.

Published in:

Journal of Medical Case Reports, 2016, v. 10, p. 1, doi. 10.1186/s13256-016-1144-8

By:

Yuki Tateno;
Ryoji Suzuki;
Yukihiro Kitamura

Publication type:

Article

Novel α-Spectrin Mutation in Trans with α-Spectrin Causing Severe Neonatal Jaundice from Hereditary Spherocytosis.

Published in:

Neonatology (16617800), 2014, v. 106, n. 4, p. 355, doi. 10.1159/000365586

By:

Nussenzveig, Roberto H.;
Christensen, Robert D.;
Prchal, Josef T.;
Yaish, Hassan M.;
agarwal, archana M.

Publication type:

Article

Erythrophagocytosis by T-cell lymphoma cells in a patient with hereditary spherocytosis post-splenectomy.

Published in:

2018

By:

Frame, Ithiel J.;
Coberly, Jared;
Fuda, Franklin S.;
Mingyi Chen

Publication type:

Case Study

Usefulness of the EMA flow cytometric test in the diagnosis of hereditary spherocytosis post-transfusion.

Published in:

British Journal of Haematology, 2017, v. 178, n. 2, p. 180, doi. 10.1111/bjh.14717

By:

Cheli, Estelle;
Roze, Jocelyn;
Garrot, Thomas;
Tagarist, Sarah;
Briandet, Claire;
Girodon, François

Publication type:

Article

A novel L1340P mutation in the ANK1 gene is associated with hereditary spherocytosis?

Published in:

British Journal of Haematology, 2014, v. 167, n. 2, p. 269, doi. 10.1111/bjh.12960

By:

Bogusławska, Dżamila M.;
Heger, Elżbieta;
Listowski, Marcin;
Wasiński, Dariusz;
Kuliczkowski, Kazimierz;
Machnicka, Beata;
Sikorski, Aleksander F.

Publication type:

Article

Poster Session Red Cell Disorders.

Published in:: 2014
Publication type:: Abstract

Severe chronic thromboembolic pulmonary hypertension in a patient after splenectomy for hereditary spherocytosis: the need for long-term surveillance and closer cooperation between haematologists and cardiologists.

Published in:

Folia Cardiologica, 2021, v. 16, n. 2, p. 130, doi. 10.5603/FC.2021.0015

By:

Klimkiewicz, Maja;
Sławiński, Grzegorz;
Faran, Anna;
Dąbrowska-Kugacka, Alicja;
Romanowicz, Grzegorz;
Kurzyna, Marcin;
Lewicka, Ewa

Publication type:

Article

Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.

Published in:

Cellular Physiology & Biochemistry (Cell Physiol Biochem Press GmbH & Co. KG), 2021, v. 55, n. 1, p. 117, doi. 10.33594/000000333

By:

Trabelsi, Nawel;
Bouguerra, Ghada;
Haddad, Faten;
Ouederni, Monia;
Darragi, Imen;
Boudrigua, Imen;
Chaouachi, Dorra;
Barmat, Mbarka;
Fouzai, Chaker;
Bejaoui, Mohamed;
Menif, Samia;
Kraiem, Imen;
Abbes, Salem

Publication type:

Article

Zinc toxicosis in a dog secondary to prolonged zinc oxide ingestion.

Published in:

2018

By:

Jia Wen Siow

Publication type:

Case Study

Correction to: Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.

Published in:

2019

By:

Park, J.;
Jeong, D.‐C.;
Yoo, J.;
Jang, W.;
Chae, H.;
Kim, J.;
Kwon, A.;
Choi, H.;
Lee, J.W.;
Chung, N.‐G.;
Kim, M.;
Kim, Y.

Publication type:

Correction Notice

Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.

Published in:

Clinical Genetics, 2016, v. 90, n. 1, p. 69, doi. 10.1111/cge.12749

By:

Park, J.;
Jeong, D.‐C.;
Yoo, J.;
Jang, W.;
Chae, H.;
Kim, J.;
Kwon, A.;
Choi, H.;
Lee, J.W.;
Chung, N.‐G.;
Kim, M.;
Kim, Y.

Publication type:

Article

Laparoscopic Subtotal Splenectomy in Children and Adolescents With Spherocytosis.

Published in:

Deutsches Ärzteblatt International, 2022, v. 119, n. 49, p. 848, doi. 10.3238/arztebl.m2022.0288

By:

Le, Melanie;
Grosse, Regine;
Elrod, Julia;
Klinke, Michaela;
Reinshagen, Konrad;
Boettcher, Michael

Publication type:

Article

Moyamoya disease associated with hereditary spherocytosis.

Published in:

2018

By:

Saraf, U. Umesh;
Arun, K.;
Sreedharan, Sapna E.;
Rajalakshmi, P.;
Sylaja, P. N.;
Umesh, Saraf U

Publication type:

Case Study

Topological Structures and Membrane Nanostructures of Erythrocytes after Splenectomy in Hereditary Spherocytosis Patients via Atomic Force Microscopy.

Published in:

Cell Biochemistry & Biophysics, 2016, v. 74, n. 3, p. 365, doi. 10.1007/s12013-016-0755-4

By:

LI, Ying;
Lu, Liyuan;
LI, Juan

Publication type:

Article

Characterization of red blood cell microcirculatory parameters using a bioimpedance microfluidic device.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66693-4

By:

Xu, Tieying;
Lizarralde-Iragorri, Maria A.;
Roman, Jean;
Ghasemi, Rasta;
Lefèvre, Jean-Pierre;
Martincic, Emile;
Brousse, Valentine;
Français, Olivier;
El Nemer, Wassim;
Le Pioufle, Bruno

Publication type:

Article

Coexistence of Gilbert Syndrome and Hereditary Spherocytosis in a Child Presenting with Extreme Jaundice.

Published in:

2014

By:

Jae Hee Lee;
Kyung Rye Moon

Publication type:

Case Study

Ventricular assist device implantation in a young patient with non-compaction cardiomyopathy and hereditary spherocytosis.

Published in:

2018

By:

Huenges, Katharina;
Panholzer, Bernd;
Cremer, Jochen;
Haneya, Assad

Publication type:

Case Study

Detection of red blood cell antibodies in mitogen-stimulated cultures from patients with hereditary spherocytosis.

Published in:

2015

By:

Zaninoni, Anna;
Vercellati, Cristina;
Imperiali, Francesca G.;
Marcello, Anna P.;
Fattizzo, Bruno;
Fermo, Elisa;
Bianchi, Paola;
Grossi, Claudia;
Cattaneo, Alessandra;
Cortelezzi, Agostino;
Zanella, Alberto;
Barcellini, Wilma

Publication type:

journal article

Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next-generation sequencing technology and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

Published in:

Molecular Medicine Reports, 2019, v. 19, n. 5, p. 3912

By:

Şener, Leyla Türker;
Aktan, Melih;
Albeniz, Gürcan;
Şener, Aziz;
Üstek, Duran;
Albeniz, Işil

Publication type:

Article

Novel compound heterozygous mutations in the SPTA1 gene, causing hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice.

Published in:

Molecular Medicine Reports, 2019, v. 19, n. 4, p. 2801

By:

Wang, Xiong;
Liu, Aiguo;
Lu, Yanjun;
Hu, Qun

Publication type:

Article

Positive predictive value of diagnosis coding for hemolytic anemias in the Danish National Patient Register.

Published in:

Clinical Epidemiology, 2016, v. 8, p. 241, doi. 10.2147/CLEP.S93643

By:

Hansen, Dennis Lund;
Overgaard, Ulrik Malthe;
Pedersen, Lars;
Frederiksen, Henrik

Publication type:

Article

Primary Bilateral Non-Hodgkin’s Lymphoma of the Adrenal Gland Presenting as Incidental Adrenal Masses.

Published in:

2015

By:

Rizzo, Christopher;
Camilleri, David James;
Betts, Alexandra;
Gatt, Andre’;
Fava, Stephen

Publication type:

Case Study

Identification of a Novel p.Q1772X ANK1 Mutation in a Korean Family with Hereditary Spherocytosis.

Published in:

PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0131251

By:

Han, Joo Hyung;
Kim, Seung;
Jang, Hoon;
Kim, So Won;
Lee, Min Goo;
Koh, Hong;
Lee, Ji Hyun

Publication type:

Article

Single-Incision Laparoscopic Splenectomy Using the Suture Suspension Technique for Splenomegaly in Children with Hereditary Spherocytosis.

Published in:

2015

By:

Li, Suolin;
Li, Meng;
Xu, Weili;
Sun, Chi;
Liu, Lin

Publication type:

journal article

Anaesthetic management of a case of hereditary spherocytosis for splenectomy and cholecystectomy.

Published in:

2014

By:

Chaithanya, Krishna;
Reddy, P. Narasimha;
Gandra, Sangamitra;
Srikanth, A.

Publication type:

Case Study

Evaluation of eosin-5-maleimide flow cytometry test in the diagnosis of hereditary spherocytosis.

Published in:

Journal of Medical Laboratory Science & Technology of South Africa, 2021, v. 3, n. 2, p. 56, doi. 10.36303/JMLSTSA.2021.3.2.75

By:

Mothi, H.;
Roodt, J. P.;
van Marle, A. C.

Publication type:

Article

Quality of life and behavioral functioning in Dutch pediatric patients with hereditary spherocytosis.

Published in:

European Journal of Pediatrics, 2014, v. 173, n. 9, p. 1217, doi. 10.1007/s00431-014-2299-1

By:

Teunissen, Myra;
Hijmans, Channa;
Cnossen, Marjon;
Bronner, Madelon;
Grootenhuis, Martha;
Peters, Marjolein

Publication type:

Article