Works matching DE "HEREDITARY spherocytosis"

Results: 72

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

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

Clinical Characteristics and Treatment Outcome of Hereditary Spherocytosis: A Single Center's Experience.

Published in:

Medical Bulletin of Sisli Etfal Hospital, 2023, v. 57, n. 4, p. 531, doi. 10.14744/SEMB.2023.60370

By:

Celik, Senanur Sanli;
Genc, Dildar Bahar;
Yildirmak, Zeynep Yildiz

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

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

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

Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.

Published in:

2019

By:

Choi, Hyoung Soo;
Choi, Qute;
Kim, Jung-Ah;
Im, Kyong Ok;
Park, Si Nae;
Park, Yoomi;
Shin, Hee Young;
Kang, Hyoung Jin;
Kook, Hoon;
Kim, Seon Young;
Kim, Soo-Jeong;
Kim, Inho;
Kim, Ji Yoon;
Kim, Hawk;
Park, Kyung Duk;
Park, Kyung Bae;
Park, Meerim;
Park, Sang Kyu;
Park, Eun Sil;
Park, Jeong-A

Publication type:

journal article

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

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

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

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

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

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

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

Combined Hereditary Spherocytosis and β-thalassemia trait: A Rare Co-existence.

Published in:

Journal of Clinical & Diagnostic Research, 2018, v. 12, n. 1, p. 9, doi. 10.7860/JCDR/2018/31302.11072

By:

SRIDEVI, HANAGANAHALLI BASAVAIAH;
SREERAM, SARASWATHY;
HEGDE, ANUPAMA;
BALANTHIMOGRU, PRASHANTHA;
CHAKRABORTI, SHRIJEET

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

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

Are the Reference Ranges and Cutoff Values of Eosin-5'-Maleimide (EMA) Binding Test for Hereditary Spherocytosis Specific for Each Age Group?

Published in:

Clinical Laboratory, 2018, v. 64, n. 6, p. 1101, doi. 10.7754/Clin.Lab.2018.180124

By:

Falay, Mesude;
Ulusan, Gul E.;
Şenes, Mehmet;
Acar, Ismail O.

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

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

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

Hereditary spherocytosis: Retrospective evaluation of 65 children.

Published in:

Turkish Journal of Pediatrics, 2018, v. 60, n. 3, p. 264, doi. 10.24953/turkjped.2018.03.005

By:

Güngör, Ali;
Yaralı, Neşe;
Fettah, Ali;
Ok-Bozkaya, İkbal;
Özbek, Namık;
Kara, Abdurrahman

Publication type:

Article

Occurrence of Wilms' tumor in a child with hereditary spherocytosis.

Published in:

Turkish Journal of Pediatrics, 2015, v. 57, n. 2, p. 206

By:

Özyörük, Derya;
Demir, Hacı Ahmet;
Emir, Suna;
Karakuş, Esra;
Tunç, Bahattin

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

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

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

Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.

Published in:

2017

By:

Kedar, Prabhakar;
Parmar, Vaishali;
Devendra, Rati;
Gupta, Vinod;
Warang, Prashant;
Madkaikar, Manisha

Publication type:

Case Study

A de novo ankyrin mutation (ANK1 Q109X) causing severe hereditary spherocytosis from preterm neonatal period.

Published in:

2017

By:

Liu, Sha;
Jiang, Hua;
Huang, Lv-Yin;
Li, Dong-Zhi

Publication type:

Case Study

A new frameshift mutation of the β-spectrin gene associated with hereditary spherocytosis.

Published in:

2017

By:

Bogusławska, Dżamila;
Heger, Elżbieta;
Machnicka, Beata;
Skulski, Michał;
Sikorski, Aleksander;
Kuliczkowski, Kazimierz;
Bogusławska, Dżamila M;
Heger, Elżbieta;
Skulski, Michał;
Sikorski, Aleksander F

Publication type:

Letter

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

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

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

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

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

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

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

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

Advances in laboratory diagnosis of hereditary spherocytosis.

Published in:

Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 7, p. 944, doi. 10.1515/cclm-2016-0738

By:

Granero Farias, Mariela

Publication type:

Article

Next-generation osmotic gradient ektacytometry for the diagnosis of hereditary spherocytosis: interlaboratory method validation and experience.

Published in:

Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 3, p. 394, doi. 10.1515/cclm-2016-0290

By:

Lazarova, Elena;
Gulbis, Béatrice;
van Oirschot, Brigitte;
van Wijk, Richard

Publication type:

Article

Eryptosis is induced by hyperthermia in hereditary spherocytosis red blood cells.

Published in:

Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 5, p. e165, doi. 10.1515/cclm-2015-0618

By:

Crisp, Renée L.;
Vota, Daiana M.;
Donato, Hugo;
García, Eliana;
Rapetti, María Cristina;
Maltaneri, Romina E.;
Vittori, Daniela C.;
Nesse, Alcira Beatriz

Publication type:

Article

Laparoscopic splenectomy for hereditary spherocytosis-preliminary report.

Published in:

European Journal of Haematology, 2016, v. 96, n. 6, p. 637, doi. 10.1111/ejh.12649

By:

Rogulski, Robert;
Adamowicz‐Salach, Anna;
Matysiak, Michał;
Piotrowski, Dariusz;
Gogolewski, Michał;
Piotrowska, Anna;
Roik, Danuta;
Kamiński, Andrzej

Publication type:

Article