Works matching DE "CONGENITAL hemolytic anemia"

Results: 129

Laparoscopic splenectomy in children. Preliminary results and comparison with the open technique.

Published in:

1995

By:

Yoshida, K;
Yamazaki, Y;
Mizuno, R;
Yamadera, H;
Hara, A;
Yoshizawa, J;
Kanai, M

Publication type:

journal article

A rare case of genetically linked primary distal renal tubular acidosis and Southeast Asian ovalocytosis.

Published in:

2020

By:

Martin, Jacqueline L.;
Davis‐Cochrane, Alexander G. J.;
Temelcos, Catherine;
Unwin, Robert J.;
Walsh, Stephen B.;
Tam, Constantine;
Goodman, David

Publication type:

Case Study

Breath-holding spells occur disproportionately more often in children with transient erythroblastopenia.

Published in:

2016

By:

Hellström Schmidt, Sanna;
Tedgård, Ulf;
Pronk, Cornelis J.H.;
Hellström Schmidt, Sanna;
Tedgård, Ulf

Publication type:

journal article

Addressing the burden of neonatal hyperbilirubinaemia in countries with significant glucose-6-phosphate dehydrogenase deficiency.

Published in:

Acta Paediatrica, 2014, v. 103, n. 11, p. 1102, doi. 10.1111/apa.12735

By:

Olusanya, Bolajoko O.;
Emokpae, Abieyuwa A.;
Zamora, Tara G.;
Slusher, Tina M.

Publication type:

Article

Effects of bilirubin and phototherapy on osmotic fragility and haematoporphyrin-induced photohaemolysis of normal erythrocytes and spherocytes.

Published in:

2005

By:

Roll, Ellen Baruzell;
Christensen, Terje;
Gederaas, Odrun A.;
Roll, Ellen Bruzell

Publication type:

journal article

Genome-Wide Association for HbA1c in Malay Identified Deletion on SLC4A1 that Influences HbA1c Independent of Glycemia.

Published in:

2020

By:

Jin-Fang Chai;
Shih-Ling Kao;
Chaolong Wang;
Victor Jun-Yu Lim;
Ing Wei Khor;
Jinzhuang Dou;
Podgornaia, Anna I.;
Chothani, Sonia;
Ching-Yu Cheng;
Sabanayagam, Charumathi;
Tien-Yin Wong;
van Dam, Rob M.;
Jianjun Liu;
Reilly, Dermot F.;
Paterson, Andrew D.;
Xueling Sim;
Chai, Jin-Fang;
Kao, Shih-Ling;
Wang, Chaolong;
Lim, Victor Jun-Yu

Publication type:

journal article

Life-threatening haemolysis induced by henna in a Sudanese child with glucose-6-phosphate dehydrogenase deficiency.

Published in:

2017

By:

Kheir, Abdelmoneim;
Gaber, Israa;
Gafer, Sara;
Ahmed, Wisal

Publication type:

Case Study

Endobiliary endoprosthesis without sphincterotomy for the treatment of biliary leakage.

Published in:

2004

By:

Katsinelos, P;
Paroutoglou, G;
Beltsis, A;
Tsolkas, P;
Arvaniti, M;
Katsiba, D;
Kalifatidis, A;
Boutsioukis, S;
Baltagiannis, S;
Georgiadou, E;
Iliadis, A;
Kapelidis, P

Publication type:

journal article

Pediatric laparoscopic splenectomy: benefits of the anterior approach.

Published in:

2004

By:

de Lagausie, P.;
Bonnard, A.;
Benkerrou, M.;
Rorlich, P.;
de Ribier, A.;
Aigrain, Y.

Publication type:

journal article

Candidate Variant Detection by Whole Exome Sequencing in Two Cases with Congenital Hemolytic Anemia.

Published in:

Experimed, 2022, v. 12, n. 1, p. S16

By:

Altindirek, Didem;
Bilici, Mustafa;
Ünal, Şule;
Tuğcu, Deniz;
Karaman, Serap;
Karakaş, Zeynep;
Sayitoğlu, Müge

Publication type:

Article

Two siblings with Majeed syndrome and neutropenia.

Published in:

Archives of Rheumatology, 2022, v. 37, n. 4, p. 638, doi. 10.46497/ArchRheumatol.2022.9437

By:

Cuceoglu, Muserref Kasap;
Batu, Ezgi Deniz;
Yildiz, Adalet Elcin;
Akca, Ummusen Kaya;
Atalay, Erdal;
Sener, Seher;
Balik, Zeynep;
Basaran, Ozge;
Bilginer, Yelda;
Ozen, Seza

Publication type:

Article

Dramatic Response of Familial Majeed Syndrome to Interleukin-1 Antagonist Therapy: Case report.

Published in:

Archives of Rheumatology, 2019, v. 34, n. 3, p. 352, doi. 10.5606/ArchRheumatol.2019.7267

By:

AL MOSAWI, Zakiya;
MADAN, Wafa;
AL MOOSAWI, Barrak;
AL-WADAEI, Sayed;
NASER, Husain;
ALI, Fuad

Publication type:

Article

Acute severe anaemia in an elderly patient with hereditary sphaerocytosis.

Published in:

2003

By:

Imhof, A.;
Kronenberg, A.;
Walter, R.B.;
Streuli, R.A.

Publication type:

journal article

Hereditary nonspherocytic hemolytic anemia caused by glucose-6-phosphate isomerase (GPI) deficiency in a Chinese patient: a case report.

Published in:

2022

By:

Zu, Yumei;
Wang, Hui;
Lin, Weijia;
Zou, Chaochun

Publication type:

journal article

Analysis of Hereditary Elliptocytosis with Decreased Binding of Eosin-5-maleimide to Red Blood Cells.

Published in:

BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/451861

By:

Shin-ichiro Suemori;
Hideho Wada;
Hidekazu Nakanishi;
Takayuki Tsujioka;
Takashi Sugihara;
Kaoru Tohyama

Publication type:

Article

Management of Anesthesia During Splenectomy and Cholecystectomy in a Pregnant Woman With Hereditary Spherocytosis.

Published in:

Journal of Guilan University of Medical Sciences, 2021, v. 30, n. 117, p. 76, doi. 10.32598/JGUMS.30.1.2

By:

Khoshrang, Hossein;
Tehran, Samaneh Ghazanfar;
Louyeh, Hourvash Ebrahimi;
Moafi Madani, Seyyed Masoud

Publication type:

Article

Parental education and the WHO neonatal G-6-PD screening program: a quarter century later.

Published in:

Journal of Perinatology, 2015, v. 35, n. 10, p. 779, doi. 10.1038/jp.2015.77

By:

Kaplan, M;
Hammerman, C;
Bhutani, V K

Publication type:

Article

Evaluating eosin-5-maleimide binding as a diagnostic test for hereditary spherocytosis in newborn infants.

Published in:

Journal of Perinatology, 2015, v. 35, n. 5, p. 357, doi. 10.1038/jp.2014.202

By:

Christensen, R D;
Agarwal, A M;
Nussenzveig, R H;
Heikal, N;
Liew, M A;
Yaish, H M

Publication type:

Article

High Frequency of Glucose-6-Phosphate Dehydrogenase Deficiency in Patients Diagnosed with Celiac Disease.

Published in:

Nutrients, 2022, v. 14, n. 9, p. 1815, doi. 10.3390/nu14091815

By:

Dore, Maria Pina;
Errigo, Alessandra;
Bibbò, Stefano;
Manca, Alessandra;
Pes, Giovanni Mario

Publication type:

Article

Hereditary Pyropoikilocytosis: A Rare But Not Uncommon Disease.

Published in:

South Dakota Medicine, 2016, v. 69, n. 5, p. 208

By:

Gali, Vasantha L.;
Lynch, Douglas W.

Publication type:

Article

A comparative evaluation of Eosin-5′-maleimide flow cytometry reveals a high diagnostic efficacy for hereditary spherocytosis.

Published in:

International Journal of Laboratory Hematology, 2016, v. 38, n. 5, p. 520, doi. 10.1111/ijlh.12533

By:

Joshi, P.;
Aggarwal, A.;
Jamwal, M.;
Sachdeva, M. U. S.;
Bansal, D.;
Malhotra, P.;
Sharma, P.;
Das, R.

Publication type:

Article

ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.

Published in:

International Journal of Laboratory Hematology, 2015, v. 37, n. 3, p. 304, doi. 10.1111/ijlh.12335

By:

King, M.‐J.;
Garçon, L.;
Hoyer, J. D.;
Iolascon, A.;
Picard, V.;
Stewart, G.;
Bianchi, P.;
Lee, S.‐H.;
Zanella, A.

Publication type:

Article

Red cell osmotic fragility in pregnant Nigerian women.

Published in:

1994

By:

Emembolu, J.O.;
Mba, E.C.

Publication type:

Letter

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

Streptococcal pyomyositis in asplenia and underlying connective tissue disease.

Published in:

Baylor University Medical Center Proceedings, 2023, v. 36, n. 4, p. 518, doi. 10.1080/08998280.2023.2210483

By:

Nguyen, John;
Singh, Pardeep;
Gajjar, Tapas

Publication type:

Article

Multigene Panel Testing Reveals Novel Variants in Hereditary Spherocytosis Patients in Türkiye.

Published in:

Turkish Journal of Hematology, 2025, v. 42, n. 1, p. 25, doi. 10.4274/tjh.galenos.2025.2024.0270

By:

Doğru, Ömer;
Alavanda, Ceren;
Demir, Şenol;
Koç, Ahmet;
Ata, Pınar

Publication type:

Article

Hereditary Elliptocytosis with Pyropoikilocytosis.

Published in:

2016

By:

Bayhan, Turan;
Ünal, Şule;
Gümrük, Fatma

Publication type:

Case Study

Immune Thrombocytopenia Resolved by Eltrombopag in a Carrier of Glucose-6-Phosphate Dehydrogenase Deficiency.

Published in:

Turkish Journal of Hematology, 2016, v. 33, p. 77, doi. 10.4274/tjh.2015.0181

By:

Scaramucci, Laura;
Niscola, Pasquale;
Palombi, Massimiliano;
Tendas, Andrea;
Giovannini, Marco;
de Fabritiis, Paolo

Publication type:

Article

Neonatal hereditary spherocytosis: a case report.

Published in:

Italian Journal of Pediatrics, 2025, v. 51, n. 1, p. 1, doi. 10.1186/s13052-025-02049-w

By:

Coramusi, Carolina;
Lucangeli, Natalia;
Vadalà, Sarah;
Parisi, Pasquale;
Scapillati, Maria Eleonora

Publication type:

Article

Hereditary stomatocytosis: an unusual cause of severe neonatal jaundice.

Published in:

2018

By:

Anselm Chi-wai Lee;
LeLe Aung;
Yeng Yoong Yip;
Cindy Ping-ping Hia;
Lee, Anselm Chi-Wai;
Aung, LeLe;
Yip, Yeng Yoong;
Hia, Cindy Ping-Ping

Publication type:

Case Study

Radionuclide Liver-Spleen Scan to Detect Splenosis.

Published in:

Indian Journal of Surgery, 2019, v. 81, n. 6, p. 602, doi. 10.1007/s12262-019-01911-6

By:

Solav, S. V.;
Patil, A. M.;
Savale, S. V.

Publication type:

Article

An Epidemic of Parvovirus B19-Induced Aplastic Crises in Pediatric Patients with Hereditary Spherocytosis Following the COVID-19 Pandemic: A Single-Center Retrospective Study.

Published in:

Children, 2025, v. 12, n. 6, p. 772, doi. 10.3390/children12060772

By:

Giordano, Paola;
Palladino, Valentina;
Lassandro, Giuseppe;
Spina, Stella;
Del Vecchio, Giovanni Carlo

Publication type:

Article

Case of Congenital Hemolytic Anemia with ATP11C and ANK1 Variants.

Published in:

Children, 2023, v. 10, n. 10, p. 1600, doi. 10.3390/children10101600

By:

Xu, Wei;
Ma, Mengmeng;
Zhao, Sai;
Yuan, Yufang;
Tian, Zhaofang

Publication type:

Article

Limits in Laparoscopic Partial Splenectomy in Children.

Published in:

Children, 2022, v. 9, n. 5, p. 605, doi. 10.3390/children9050605

By:

Tomuschat, Christian;
Aftzoglou, Michail;
Hagens, Johanna;
Boettcher, Michael;
Reinshagen, Konrad

Publication type:

Article

Mechanisms Linking Red Blood Cell Disorders and Cardiovascular Diseases.

Published in:

BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/682054

By:

Mozos, Ioana

Publication type:

Article

Familial thrombotic microangiopathy in a child with coenzyme Q10 deficiency-associated glomerulopathy.

Published in:

Pediatric Nephrology, 2025, v. 40, n. 2, p. 377, doi. 10.1007/s00467-024-06496-1

By:

Lin, Kyle Ying-kit;
Lam, Ching-wan;
Chan, Eugene Yu-hin;
Lee, Mianne;
Chung, Brian Hon-yin;
Fung, Cheuk-wing;
Rodenburg, Richard;
Licht, Christoph;
Lap-tak MA, Alison

Publication type:

Article

Identification of Rh alloantibody in Thalassaemia Patients.

Published in:

Journal of Medicine, 2016, v. 17, n. 2, p. 79, doi. 10.3329/jom.v17i2.30069

By:

SULTANA, NAHID;
RAHMAN, ATIAR;
EASMIN, FATEMA;
HOQUE, MD. MAZHARUL;
ISLAM, KASHFIA;
SHORMIN, SONIA;
BISWAS5, JOLLY

Publication type:

Article

Laparoscopic Partial Splenectomy: A Critical Appraisal of an Emerging Technique. A Review of the First 457 Published Cases.

Published in:

2021

By:

Romboli, Andrea;
Annicchiarico, Alfredo;
Morini, Andrea;
Castro Ruiz, Carolina;
Pagliai, Lorenzo;
Montali, Filippo;
Costi, Renato

Publication type:

journal 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

Splenic infarction after Epstein-Barr virus infection in a patient with hereditary spherocytosis: a case report and literature review.

Published in:

2022

By:

Ma, Zhongwu;
Wang, Zhejin;
Zhang, Xiaodan;
Yu, Haibo

Publication type:

journal 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

Post-transfusion Hypertension and Seizure in Congenital Hemolytic anemia: A Case Report and Literature Review.

Published in:

Journal of Tropical Pediatrics, 2014, v. 60, n. 3, p. 253, doi. 10.1093/tropej/fmu003

By:

Ngim, Chin Fang;
Ng, Chen Siew;
Lai, Nai Ming

Publication type:

Article

Glucose-6-Phosphate Dehydrogenase Deficiency: A Single-Center Experience.

Published in:

Turkish Archives of Pediatrics, 2022, v. 57, n. 1, p. 104, doi. 10.5152/TurkArchPediatr.2022.21195

By:

Al-Mendalawi, Mahmood D.

Publication type:

Article

Glucose 6 phosphate dehydrogenase deficiency: A single-center experience.

Published in:

Turkish Archives of Pediatrics, 2021, v. 56, n. 3, p. 245, doi. 10.5152/TurkArchPediatr.2021.20042

By:

Kılıç, Mehmet Akif;
Özdemir, Gül Nihal;
Tahtakesen, Tuba Nur;
Uysalol, Ezgi Paslı;
Bayram, Cengiz;
Ayçiçek, Ali;
Aydoğan, Gönül

Publication type:

Article

Significance of teardrop cells in peripheral blood smears.

Published in:

Journal of Laboratory Medicine / Laboratoriums Medizin, 2014, p. 1, doi. 10.1515/labmed-2014-0005

By:

Gütgemann, Ines;
Heimpel, Hermann;
Nebe, Carl Thomas

Publication type:

Article

A novel homozygous missense variant p.D339N in the PKLR gene correlates with pyruvate kinase deficiency in a Pakistani family: a case report.

Published in:

2022

By:

Rehman, Atta Ur;
Rashid, Abdur;
Hussain, Zubair;
Shah, Khadim

Publication type:

journal article

Hereditary Spherocytosis Unmasked by Human Parvovirus B19 Induced Aplastic Crisis in a Family.

Published in:

Iranian Journal of Medical Sciences, 2015, v. 40, n. 5, p. 461

By:

Alavi, Samin;
Arabi, Nahid;
Yazdi, Mohammad Kaji;
Arzanian, Mohammad Taghi;
Zohrehbandian, Farahnaz

Publication type:

Article

An infant with chronic hemolytic anemia.

Published in:

2014

By:

Tüysüz, Gülen;
Özdemir, Gül Nihal;
Celkan, Tiraje

Publication type:

Case Study

Majeed Syndrome: Five Cases With Novel Mutations From Unrelated Families in India With a Review of Literature.

Published in:

2021

By:

Chavan, Pallavi Pimpale;
Aksentijevich, Ivona;
Daftary, Aditya;
Panwala, Hiren;
Khemani, Chetna;
Khan, Archana;
Khubchandani, Raju

Publication type:

journal article

Overview on Hereditary Spherocytosis Diagnosis.

Published in:

International Journal of Laboratory Hematology, 2025, v. 47, n. 1, p. 18, doi. 10.1111/ijlh.14376

By:

Polizzi, A.;
Dicembre, L. P.;
Failla, C.;
Matola, T. Di;
Moretti, M.;
Ranieri, S. Chiatamone;
Papa, F.;
Cenci, A. M.;
Buttarello, M.

Publication type:

Article