1. Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency. Issue 1 (28th November 2018) Authors: Bianchi, Paola; Fermo, Elisa; Glader, Bertil; Kanno, Hitoshi; Agarwal, Archana; Barcellini, Wilma; Eber, Stefan; Hoyer, James D.; Kuter, David J.; Maia, Tabita Magalhães; Mañu‐Pereira, Maria del Mar; Kalfa, Theodosia A.; Pissard, Serge; Segovia, José‐Carlos; van Beers, Eduard; Gallagher, Patrick ... Journal: American journal of hematology Issue: Volume 94:Issue 1(2019:Jan.) Page Start: 149 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Hemoglobin C trait accentuates erythrocyte dehydration in hereditary xerocytosis. Issue 8 (25th January 2017) Authors: Yang, Elizabeth; Voelkel, Erin B.; Lezon‐Geyda, Kimberly; Schulz, Vincent P.; Gallagher, Patrick G. Journal: Pediatric blood & cancer Issue: Volume 64:Issue 8(2017) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genotype‐phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency. Issue 5 (6th March 2020) Authors: Bianchi, Paola; Fermo, Elisa; Lezon‐Geyda, Kimberly; van Beers, Eduard J.; Morton, Holmes D.; Barcellini, Wilma; Glader, Bertil; Chonat, Satheesh; Ravindranath, Yaddanapudi; Newburger, Peter E.; Kollmar, Nina; Despotovic, Jenny M.; Verhovsek, Madeleine; Sharma, Mukta; Kwiatkowski, Janet L.; Kuo, ... Journal: American journal of hematology Issue: Volume 95:Issue 5(2020:May) Page Start: 472 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. The genetic basis of asymptomatic codon 8 frame‐shift (HBB:c25_26delAA) β0‐thalassaemia homozygotes. (13th January 2016) Authors: Jiang, Zhihua; Luo, Hong‐yuan; Huang, Shengwen; Farrell, John J.; Davis, Lance; Théberge, Roger; Benson, Katherine A.; Riolueang, Suchada; Viprakasit, Vip; Al‐Allawi, Nasir A.S.; Ünal, Sule; Gümrük, Fatma; Akar, Nejat; Başak, A. Nazli; Osorio, Leonor; Badens, Catherine; Pissard, Serge; Joly, Phil... Journal: British journal of haematology Issue: Volume 172:Number 6(2016) Page Start: 958 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Summary of Joint European Hematology Association (EHA) and EuroBloodNet Recommendations on Diagnosis and Treatment of Methemoglobinemia. Issue 12 (17th December 2021) Authors: Iolascon, Achille; Andolfo, Immacolata; Russo, Roberta; Barcellini, Wilma; Fermo, Elisa; Toldi, Gergely; Ghirardello, Stefano; Rees, Davis; Van Wijk, Richard; Kattamis, Antonis; Gallagher, Patrick G.; Roy, Noemi; Taher, Ali; Mohty, Razan; Kulozik, Andreas; De Franceschi, Lucia; Gambale, Antonella... Other Names: other. Journal: HemaSphere Issue: Volume 5:Issue 12(2021) Page Start: e660 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. D‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. Issue 1 (8th October 2021) Authors: Werner, Kelly M.; Cox, Allison J.; Qian, Emily; Jain, Preti; Ji, Weizhen; Tikhonova, Irina; Castaldi, Christopher; Bilguvar, Kaya; Knight, James; Ferdinandusse, Sacha; Fawaz, Rima; Jiang, Yong‐Hui; Gallagher, Patrick G.; Bizzarro, Matthew; Gruen, Jeffrey R.; Bale, Allen; Zhang, Hui Journal: American journal of medical genetics Issue: Volume 188:Issue 1(2022) Page Start: 357 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Histone Acetyltransferases p300 and CBP Coordinate Distinct Chromatin Remodeling Programs in Vascular Smooth Muscle Plasticity. Issue 23 (3rd May 2022) Authors: Chakraborty, Raja; Ostriker, Allison C.; Xie, Yi; Dave, Jui M.; Gamez-Mendez, Ana; Chatterjee, Payel; Abu, Yaw; Valentine, Jake; Lezon-Geyda, Kimberly; Greif, Daniel M.; Schulz, Vincent P.; Gallagher, Patrick G.; Sessa, William C.; Hwa, John; Martin, Kathleen A. Journal: Circulation Issue: Volume 145:Issue 23(2022) Page Start: 1720 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV: Insights Into the Variable Clinical Severity. Issue 6 (August 2018) Authors: Ravindranath, Yaddanapudi; Johnson, Robert M.; Goyette, Gerard; Buck, Steven; Gadgeel, Manisha; Gallagher, Patrick G. Journal: Journal of pediatric hematology/oncology Issue: Volume 40:Issue 6(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Human and murine erythropoiesis. Issue 3 (May 2015) Authors: An, Xiuli; Schulz, Vincent P.; Mohandas, Narla; Gallagher, Patrick G. Journal: Current opinion in hematology Issue: Volume 22:Issue 3(2015:May) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Hepatic Malignancy in an Infant with Wolf–Hirschhorn Syndrome. (4th May 2017) Authors: Rutter, Sara; Morotti, Raffaella A; Peterec, Steven; Gallagher, Patrick G. Journal: Fetal and pediatric pathology Issue: Volume 36:Number 3(2017) Page Start: 256 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗