Works about MACROCYTIC anemia

Results: 146

Oesophagogastric reconnection is possible.

Published in:

Pediatric Surgery International, 2014, v. 30, n. 5, p. 511, doi. 10.1007/s00383-014-3483-0

By:

Maignan, A.;
Bonnard, A.;
Hery, G.;
Guys, J.;
Lagausie, P.

Publication type:

Article

Novel Homozygous Variant in the SLC19A2 Gene Causing Thiamine Responsive Megaloblastic Anemia Syndrome: A Disease to Be Considered in Diabetes Clinics.

Published in:

Endocrinology Research & Practice, 2024, v. 28, n. 4, p. 236, doi. 10.5152/erp.2024.473

By:

Helvaci, Burcak Cavnar;
Saat, Hanife;
Hepsen, Sema;
Helvaci, Özant;
Cakal, Erman

Publication type:

Article

In the era of automation and molecular techniques, is peripheral blood smear examination getting redundant?

Published in:

International Journal of Advanced Medical & Health Research, 2022, v. 9, n. 1, p. 1, doi. 10.4103/ijamr.ijamr_104_22

By:

Basu, Debdatta

Publication type:

Article

Spontaneous resolution of macrocytic anemia: old disease revisited.

Published in:

2012

By:

Imashuku, Shinsaku;
Kudo, Naoko;
Kaneda, Shigehiro

Publication type:

Case Study

Efficient detection of somatic UBA1 variants and clinical scoring system predicting patients with variants in VEXAS syndrome.

Published in:

Rheumatology, 2024, v. 63, n. 8, p. 2056, doi. 10.1093/rheumatology/kead425

By:

Maeda, Ayaka;
Tsuchida, Naomi;
Uchiyama, Yuri;
Horita, Nobuyuki;
Kobayashi, Satoshi;
Kishimoto, Mitsumasa;
Kobayashi, Daisuke;
Matsumoto, Haruki;
Asano, Tomoyuki;
Migita, Kiyoshi;
Kato, Ayaka;
Mori, Ichiro;
Morita, Hiroyuki;
Matsubara, Akihiro;
Marumo, Yoshiaki;
Ito, Yuji;
Machiyama, Tomoaki;
Shirai, Tsuyoshi;
Ishii, Tomonori;
Kishibe, Mari

Publication type:

Article

Three UBA1 clones for a unique VEXAS syndrome.

Published in:

2024

By:

Podvin, Benjamin;
Cleenewerck, Nathalie;
Nibourel, Olivier;
Marceau-Renaut, Alice;
Roynard, Pauline;
Preudhomme, Claude;
Duployez, Nicolas;
Terriou, Louis

Publication type:

Case Study

Influence of HLA polymorphisms on clinical features of VEXAS syndrome: a potential epistatic mechanism.

Published in:

2023

By:

Lucchino, Bruno;
Finucci, Annacarla;
Ghellere, Francesco;
Bortolotti, Maria Elena;
Tedesco, Andrea;
Lombardi, Sara

Publication type:

Case Study

VEXAS syndrome-related AA amyloidosis: a case report.

Published in:

2022

By:

Euvrard, Romain;
Fournier, Thomas;
Georgescu, Dana;
Bourbon, Estelle;
Sujobert, Pierre;
Lega, Jean Christophe;
Adelaide, Leopold

Publication type:

Case Study

Atypical splice-site mutations causing VEXAS syndrome.

Published in:

2021

By:

Templé, Marie;
Duroyon, Eugénie;
Croizier, Carolyne;
Rossignol, Julien;
Huet, Thomas;
Friedrich, Chloé;
Zalmai, Loria;
Priollet, Pascal;
Hayem, Gilles;
Tournillhac, Olivier;
Guenno, Guillaume Le;
Hermine, Olivier;
Terrier, Benjamin;
Kosmider, Olivier

Publication type:

Case Study

A case of VEXAS syndrome manifesting as Kikuchi-Fujimoto disease, relapsing polychondritis, venous thromboembolism and macrocytic anaemia.

Published in:

2021

By:

Lee, Shang Ming Samuel;
Fan, Bingwen Eugene;
Lim, Joel Hua-Liang;
Goh, Liuh Ling;
Lee, Joyce Siong See;
Koh, Li Wearn

Publication type:

Case Study

Positive ultrasound halo sign of temporal arteries due to amyloidosis.

Published in:

2019

By:

Collada, Juan Molina;
Bravo-Burguillos, Elena Ruíz;
Monjo, Irene;
Bonilla, Gema;
Fernández, Elisa;
Balsa, Alejandro;
Miguel, Eugenio De

Publication type:

Case Study

A surfacing problem.

Published in:

Ibnosina Journal of Medicine & Biomedical Sciences, 2012, v. 4, n. 3, p. 103, doi. 10.4103/1947-489X.210758

By:

Chan, Howard H.;
Chan, Anthony K.;
Lau, Keith K.

Publication type:

Article

Runner's anemia.

Published in:

2001

By:

Dang, Chi V.;
Dang, C V

Publication type:

journal article

Megaloblastic anaemia associated with the oral contraceptive pill.

Published in:

1974

By:

Meguid, Michael M.;
Loebl, Walter Y.;
Meguid, M M;
Loebl, W Y

Publication type:

journal article

Low Frequency of Folate and Vitamin B12 Deficiency in Patients with Marked Macrocytic Anemia.

Published in:

2022

By:

Soffer, Shelly;
Efros, Orly;
Levin, Matthew A.;
Freeman, Robert;
Zimlichman, Eyal;
Reich, David L.;
Klang, Eyal

Publication type:

journal article

Vitamin B12 deficiency as a cause of severe neurological symptoms in breast fed infant – a case report.

Published in:

Italian Journal of Pediatrics, 2020, v. 46, n. 1, p. 1, doi. 10.1186/s13052-020-0804-x

By:

Dubaj, Cezary;
Czyż, Katarzyna;
Furmaga-Jabłońska, Wanda

Publication type:

Article

Profile of anemia in acute lymphoblastic leukemia patients on maintenance therapy and the effect of micronutrient supplementation.

Published in:

2020

By:

Pattnaik, Jogamaya;
Kayal, Smita;
Dubashi, Biswajit;
Basu, Debdatta;
Vinod, K. V.;
Nandeesha, H.;
Madasamy, Ponraj;
Kumar, Ranjith C. S.;
Pillai, Unni S.;
Jadhav, Naresh

Publication type:

journal article

ADAMTS-13 deficiency: can it cause chronic renal failure?

Published in:

Nephrology Dialysis Transplantation, 2011, v. 26, n. 2, p. 742, doi. 10.1093/ndt/gfq644

By:

Bramham, Kate;
Hilton, Rachel;
Horsfield, Catherine;
McDonald, Vickie;
Camilleri, Raymond;
Hunt, Beverley J.

Publication type:

Article

Caracterización de la anemia en ancianos hospitalizados en el Hospital Clínico Quirúrgico Docente León Cuervo Rubio.

Published in:

Revista de Ciencias Médicas de Pinar del Río, 2024, v. 28, n. 1, p. 1

By:

Liana Carbó-Rodríquez, Heidy;
Juvier-Chamizo, Lorna;
Junco-Labrador, Liyanis;
Alejandro Herrera-Horta, Guillermo;
León-Amado, Liliam

Publication type:

Article

Gastric Neuroendocrine Tumor Type 1 Associated with Autoimmune Polyglandular Syndrome Type 3B: A Case Report.

Published in:

Neuroendocrinology, 2012, v. 96, p. 41

By:

Kruljac, I.;
Mirošević, G.;
Ljubičić, N.;
Vrkljan, M.

Publication type:

Article

Pyrexia in a Patient with Megaloblastic Anemia: A Case Report and Literature Review.

Published in:

Iranian Journal of Medical Sciences, 2013, v. 38, p. 198

By:

Manuel, Kevin;
Padhi, Somanath;
Varghese, Renu GÂ¿Boy

Publication type:

Article

Vitamin B<sub>12</sub> Deficiency with the Absence of Anemia in Young and Middle-Aged Population.

Published in:

UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2014, v. 24, n. 3, p. 190, doi. 10.4999/uhod.14459

By:

KARA, Atilla;
ELIACIK, Eylem;
BUYUKASIK, Yahya;
OZCEBE, Osman I.;
HAZNEDAROGLU, Ibrahim;
AKSU, Salih;
BEKTAS, Ozlen;
GOKER, Hakan;
SAYINALP, Nilgun

Publication type:

Article

Pak2 Regulates Hematopoietic Progenitor Cell Proliferation, Survival, and Differentiation.

Published in:

Stem Cells, 2015, v. 33, n. 5, p. 1630, doi. 10.1002/stem.1951

By:

Zeng, Yi;
Broxmeyer, Hal E.;
Staser, Karl;
Chitteti, Brahmananda Reddy;
Park, Su-Jung;
Hahn, Seongmin;
Cooper, Scott;
Sun, Zejin;
Jiang, Li;
Yang, XianLin;
Yuan, Jin;
Kosoff, Rachelle;
Sandusky, George;
Srour, Edward F.;
Chernoff, Jonathan;
Clapp, D. Wade

Publication type:

Article

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.

Published in:

2020

By:

Bedin, Mathilda;
Boyer, Olivia;
Servais, Aude;
Yong Li;
Villoing-Gaudé, Laure;
Tête, Marie-Josephe;
Cambier, Alexandra;
Hogan, Julien;
Baudouin, Veronique;
Krid, Saoussen;
Bensman, Albert;
Lammens, Florie;
Louillet, Ferielle;
Ranchin, Bruno;
Vigneau, Cecile;
Bouteau, Iseline;
Isnard-Bagnis, Corinne;
Mache, Christoph J.;
Schäfer, Tobias;
Pape, Lars

Publication type:

journal article

X-linked macrocytic dyserythropoietic anemia in females with an ALAS2 mutation.

Published in:

Journal of Clinical Investigation, 2015, v. 125, n. 4, p. 1665, doi. 10.1172/JCI78619

By:

Sankaran, Vijay G.;
Ulirsch, Jacob C.;
Tchaikovskii, Vassili;
Ludwig, Leif S.;
Wakabayashi, Aoi;
Kadirvel, Senkottuvelan;
Lindsley, R. Coleman;
Bejar, Rafael;
Shi, Jiahai;
Lovitch, Scott B.;
Bishop, David F.;
Steensma, David P.

Publication type:

Article

Clinical evaluation of severe anemia in pregnancy with special reference to macrocytic anemia.

Published in:

Journal of Obstetrics & Gynaecology Research, 2012, v. 38, n. 1, p. 203, doi. 10.1111/j.1447-0756.2011.01679.x

By:

Tripathi, Reva;
Tyagi, Shakun;
Singh, Tejinder;
Dixit, Amrapali;
Manju;
Mala, Y. M.

Publication type:

Article

A Vexing diagnosis: A case report on VEXAS syndrome.

Published in:

Canadian Journal of Respiratory, Critical Care, & Sleep Medicine, 2025, v. 9, n. 2, p. 100, doi. 10.1080/24745332.2025.2455402

By:

Bryan, Craig;
Fidler, Lee

Publication type:

Article

The Role of Folate in Reducing Chronic and Developmental Disease Risk: An Overview.

Published in:

Journal of Food Science (Wiley-Blackwell), 2004, v. 69, n. 1, p. SNQ55, doi. 10.1111/j.1365-2621.2004.tb17887.x

By:

CAUDILL, MARIE

Publication type:

Article

Behind the Skin: A Rare Case of Scurvy-Associated Megaloblastic Anemia.

Published in:

Clinical Medicine Insights: Case Reports, 2019, v. 12, p. N.PAG, doi. 10.1177/1179547619849036

By:

Alhatem, Albert;
Cai, Donghong

Publication type:

Article

Behind the Skin: A Rare Case of Scurvy-Associated Megaloblastic Anemia.

Published in:

Clinical Medicine Insights: Case Reports, 2019, n. 12, p. N.PAG, doi. 10.1177/1179547619849036

By:

Alhatem, Albert;
Cai, Donghong

Publication type:

Article

Clinico-Haematological Profile of Megaloblastic Anaemia.

Published in:

Journal of Institute of Medicine Nepal (JIOMN), 2014, v. 36, n. 1, p. 38, doi. 10.59779/jiomnepal.570

By:

Hirachand, S.;
Singh, R.;
Gurung, P.;
Thapa, R.

Publication type:

Article

c-MVC Amplification in Acute Myelogenous Leukemia Evolving from Double Minutes (dmins) to Homogeneously Staining Region (hsr).

Published in:

Journal of the Association of Genetic Technologists, 2014, v. 40, n. 2, p. 64

By:

Sayedian, Farzaneh;
Senft, Jamie R.;
Spruill, Michelle D.;
Wenger, Sharon L.;
Vos, Jeffrey A.

Publication type:

Article

Cobalamin (vitamin B12) metabolism during pregnancy

Published in:

2004

By:

Pardo, J.;
Gindes, L.;
Orvieto, R.

Publication type:

journal article

Breath-holding spell and macrocytic anaemia in a toddler.

Published in:

British Journal of Haematology, 2014, v. 166, n. 2, p. 156, doi. 10.1111/bjh.12927

By:

Ramachandran, Shanti;
Alessandri, Angela;
Price, James;
Balasubramaniam, Shanti

Publication type:

Article

Gaucher disease and myelodysplastic syndrome with isolated del(5q).

Published in:

British Journal of Haematology, 2014, v. 165, n. 2, p. 164, doi. 10.1111/bjh.12798

By:

Villarrubia, Jesús;
Rodríguez‐Gambarte, Juan D.;
Abalo, Lorena;
Vallés, Ana;
Alonso‐Domínguez, Juan Manuel;
Velasco‐Rodríguez, Diego

Publication type:

Article

Evaluation of mean corpuscular volume among anemic people with HIV in North America following ART initiation.

Published in:

AIDS Research & Therapy, 2024, v. 21, n. 1, p. 1, doi. 10.1186/s12981-024-00641-4

By:

Lang, Raynell;
Coburn, Sally B.;
Gill, M. John;
Justice, Amy C.;
Grossman, Jennifer;
Gebo, Kelly A.;
Horberg, Michael A.;
Mayor, Angel M.;
Silverberg, Michael J.;
McGinnis, Kathleen A.;
Hogan, Brenna;
Moore, Richard D.;
Althoff, Keri N.

Publication type:

Article

Comment on: Bilateral macular hemorrhage due to megaloblastic anemia: A rare case report.

Published in:

2016

By:

Goel, Neha

Publication type:

Letter

Homocystinuria due to cystathionine beta-synthase deficiency associated with megaloblastic anaemia.

Published in:

2001

By:

Ishida, S;
Isotani, H;
Furukawa, K;
Kuhara, T

Publication type:

Case Study

Clinical images: VEXAS syndrome presenting as treatment‐refractory polyarteritis nodosa.

Published in:

2022

By:

Itagane, Masaki;
Teruya, Hiroyuki;
Kato, Tomohiro;
Tsuchida, Naomi;
Maeda, Ayaka;
Kirino, Yohei;
Uchiyama, Yuri;
Matsumoto, Naomichi;
Kinjo, Mitsuyo

Publication type:

Case Study

Hematological Profile of Women in Pregnancy in a Hilly District of Himachal Pradesh.

Published in:

Indian Journal of Community Health, 2020, v. 32, n. 3, p. 506, doi. 10.47203/ijch.2020.v32i03.008

By:

Sharma, Anuj;
Vohra, Jai Gopal;
Behal, Manisha;
Bansal, Sneha

Publication type:

Article

Delayed globin synthesis leads to excess heme and the macrocytic anemia of Diamond Blackfan anemia and del(5q) myelodysplastic syndrome.

Published in:

Science Translational Medicine, 2016, v. 8, n. 338, p. 1, doi. 10.1126/scitranslmed.aaf3006

By:

Zhantao Yang;
Keel, Siobán B.;
Akiko Shimamura;
Li Liu;
Gerds, Aaron T.;
Li, Henry Y.;
Wood, Brent L.;
Scott, Bart L.;
Abkowitz, Janis L.

Publication type:

Article

Megaloblastic anemia-related iron overload and erythroid regulators: a case report.

Published in:

2021

By:

Vallet, Nicolas;
Delaye, Jean-Baptiste;
Ropert, Martine;
Foucault, Amélie;
Ravalet, Noémie;
Deriaz, Sophie;
Chalopin, Thomas;
Blasco, Hélène;
Maillot, François;
Hérault, Olivier;
Gyan, Emmanuel

Publication type:

journal article

Study of Anaemia in Children with Severe Acute Malnutrition.

Published in:

Journal of Nepal Paediatric Society, 2017, v. 37, n. 3, p. 250, doi. 10.3126/jnps.v37i3.18480

By:

D., Dwivedi;
V., Singh;
J., Singh;
S., Sharma

Publication type:

Article

Imerslund-Gräsbeck syndrome in a child with a novel compound heterozygous mutations in the AMN gene: a case report.

Published in:

Italian Journal of Pediatrics, 2024, v. 50, n. 1, p. 1, doi. 10.1186/s13052-024-01757-z

By:

Zhang, Dedong;
Liu, Siying;
Xi, Bixin;
Zhu, Yongbing;
Chen, Yu;
Zhang, Jiasi;
Liu, Aiguo

Publication type:

Article

An Italian case series' description of thiamine responsive megaloblastic anemia syndrome: importance of early diagnosis and treatment.

Published in:

Italian Journal of Pediatrics, 2023, v. 49, n. 1, p. 1, doi. 10.1186/s13052-023-01553-1

By:

Di Candia, Francesca;
Di Iorio, Valentina;
Tinto, Nadia;
Bonfanti, Riccardo;
Iovino, Claudio;
Rosanio, Francesco Maria;
Fedi, Ludovica;
Iafusco, Fernanda;
Arrigoni, Francesca;
Malesci, Rita;
Simonelli, Francesca;
Rigamonti, Andrea;
Franzese, Adriana;
Mozzillo, Enza

Publication type:

Article

Effects of benzo(a)pyrene on blood components, tumor markers, and oxidative status in mice.

Published in:

Toxicological & Environmental Chemistry, 2012, v. 94, n. 1, p. 136, doi. 10.1080/02772248.2011.630149

By:

Hegazy, A.M.;
Bakry, H.H.;
El-Shawarby, R.M.;
Abou-Salem, M.E.;
El-Aleem, N.M. Abd;
Nasr, S.M.

Publication type:

Article

Thiamine responsive megaloblastic anemia: a novel SLC19A2 compound heterozygous mutation in two siblings.

Published in:

Pediatric Diabetes, 2013, v. 14, n. 5, p. 384, doi. 10.1111/j.1399-5448.2012.00921.x

By:

Mozzillo, Enza;
Melis, Daniela;
Falco, Mariateresa;
Fattorusso, Valentina;
Taurisano, Roberta;
Flanagan, Sarah E;
Ellard, Sian;
Franzese, Adriana

Publication type:

Article

Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia.

Published in:

Pediatric Diabetes, 2012, v. 13, n. 4, p. 307, doi. 10.1111/j.1399-5448.2012.00855.x

By:

Shaw-Smith, Charles;
Flanagan, Sarah E;
Patch, Ann-Marie;
Grulich-Henn, Juergen;
Habeb, Abdelhadi M;
Hussain, Khalid;
Pomahacova, Renata;
Matyka, Krystyna;
Abdullah, Mohamed;
Hattersley, Andrew T;
Ellard, Sian

Publication type:

Article

Widespread red oral lesions.

Published in:

2013

By:

Flores, Isadora Luana;
Santos-Silva, Alan Roger;
Coletta, Ricardo D.;
Vargas, Pablo Agustin;
Lopes, Marcio A.

Publication type:

Case Study

Imerslund-Gräsbeck syndrome in a 15-year-old German girl caused by compound heterozygous mutations in CUBN.

Published in:

2008

By:

Hauck, Fabian H.;
Tanner, Stephan M.;
Henker, Jobst;
Laass, Martin W.

Publication type:

journal article