Hemoglobin M disease (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hemoglobin M disease" in English language version.

refsWebsite

Global rank English rank

28nih.gov

4^th place

21worldcat.org

5^th place

18doi.org

2^nd place

8semanticscholar.org

11^th place

8^th place

3sciencedirect.com

149^th place

178^th place

2handle.net

102^nd place

76^th place

1sagepub.com

731^st place

638^th place

1wiley.com

222^nd place

297^th place

1karger.com

4,489^th place

4,454^th place

1harvard.edu

18^th place

17^th place

doi.org

Alonso-Ojembarrena, A. (2016). "Hemoglobin M Disease as a Cause of Cyanosis in a Newborn". Journal of Pediatric Hematology/Oncology. 38 (3): 173–175. doi:10.1097/MPH.0000000000000489. PMID 26694193. S2CID 26848356 – via PubMed.
Iolascon, Achille; Bianchi, Paola; Andolfo, Immacolata; Russo, Roberta; Barcellini, Wilma; Fermo, Elisa; Toldi, Gergely; Ghirardello, Stefano; Rees, Davis; Van Wijk, Richard; Kattamis, Antonis (2021-09-23). "Recommendations for diagnosis and treatment of methemoglobinemia". American Journal of Hematology. 96 (12): 1666–1678. doi:10.1002/ajh.26340. hdl:1887/3249335. ISSN 0361-8609. PMC 9291883. PMID 34467556. S2CID 237377613.
Picca, Andrew; Ruthford, Mason; Ghanim, Majd T.; Sims, Morgan; Kanter, Julie (2019-08-20). "Diagnosis of Hemoglobin M Disease in a Toddler Presenting With Hypoxemia and Hemolysis". Clinical Pediatrics. 58 (11–12): 1345–1348. doi:10.1177/0009922819870555. ISSN 0009-9228. PMID 31431070. S2CID 201115221.
Arceci, Robert J.; Hann, Ian M.; Smith, Owen P., eds. (2006-08-31). Pediatric Hematology. Blackwell Publishing. doi:10.1002/9780470987001. ISBN 9780470987001.
Sangkitporn, S. K.; Eksiri, L.; Sangnoi, A.; Duangruang, S.; Dumbua, A.; Rattanakittisophon, K.; Sangkitporn, S. (2009). "Identification of beta-globin gene mutations in Thailand using an automated fluorescence-based DNA sequencer". International Journal of Laboratory Hematology. 31 (5): 521–527. doi:10.1111/j.1751-553X.2008.01072.x. ISSN 1751-553X. PMID 18498386. S2CID 31589532.
Rehman, Habib Ur (2001). "Methemoglobinemia". Western Journal of Medicine. 175 (3): 193–196. doi:10.1136/ewjm.175.3.193. ISSN 0093-0415. PMC 1071541. PMID 11527852.
Patnaik, Sibabratta; Natarajan, Manivachagan Muthappa; James, Ebor Jacob; Ebenezer, Kala (2014). "Methylene blue unresponsive methemoglobinemia". Indian Journal of Critical Care Medicine. 18 (4): 253–255. doi:10.4103/0972-5229.130582. ISSN 0972-5229. PMC 4033863. PMID 24872659.
Göttgens, Eva-Leonne; Baks, Kristian; Harteveld, Cornelis L.; Goossens, Kristel; van Gammeren, Adriaan J. (2021). "Cyanosis, hemolysis, decreased HbA1c and abnormal co-oximetry in a patient with hemoglobin M Saskatoon [HBB:c.190C > T p.His64Tyr]". Hematology (Amsterdam, Netherlands). 26 (1): 914–918. doi:10.1080/16078454.2021.1999048. hdl:1887/3249333. ISSN 1607-8454. PMID 34789072. S2CID 244346360.
Percy, Melanie J.; Lappin, Terry R. (2008). "Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency". British Journal of Haematology. 141 (3): 298–308. doi:10.1111/j.1365-2141.2008.07017.x. ISSN 1365-2141. PMID 18318771. S2CID 36408296.
Özsoylu, S. (1972). "Congenital Methemoglobinemia Due to Hemoglobin M". Acta Haematologica. 47 (4): 225–232. doi:10.1159/000208528. ISSN 0001-5792. PMID 4625305.
Rangan, Aruna; Savedra, Michelle E.; Dergam-Larson, Camila; Swanson, Kenneth C.; Szuberski, Jessica; Go, Ronald S.; Porter, Tavanna R.; Brunker, Sarah E.; Shi, Min; Nguyen, Phuong L.; Hoyer, James D. (August 2021). "Interpreting sulfhemoglobin and methemoglobin in patients with cyanosis: An overview of patients with M-hemoglobin variants". International Journal of Laboratory Hematology. 43 (4): 837–844. doi:10.1111/ijlh.13581. ISSN 1751-553X. PMID 34092029. S2CID 235362094.
Rastogi, Loveena; Langer, Sabina; Radhakrishnan, Nita; Saxena, Renu; Kotwal, Jyoti (2020-09-30). "Hb-M Hyde Park: a rare cause of cyanosis arising from a de novo mutation". Blood Research. 55 (3): 177–180. doi:10.5045/br.2020.2020084. ISSN 2287-979X. PMC 7536569. PMID 32747614.
Spears, Frances; Banerjee, Arnab (June 2008). "Hemoglobin M variant and congenital methemoglobinemia: methylene blue will not be effective in the presence of hemoglobin M". Canadian Journal of Anaesthesia. 55 (6): 391–392. doi:10.1007/BF03021499. ISSN 0832-610X. PMID 18566207. S2CID 46308991.
Vichinsky, E. P.; Lubin, B. H. (May 1980). "Unstable hemoglobins, hemoglobins with altered oxygen affinity, and m-hemoglobins". Pediatric Clinics of North America. 27 (2): 421–428. doi:10.1016/s0031-3955(16)33859-7. ISSN 0031-3955. PMID 7383714.
Mihailescu, Mihaela-Rita; Russu, Irina M. (2001-03-27). "A signature of the T → R transition in human hemoglobin". Proceedings of the National Academy of Sciences of the United States of America. 98 (7): 3773–3777. Bibcode:2001PNAS...98.3773M. doi:10.1073/pnas.071493598. ISSN 0027-8424. PMC 31128. PMID 11259676.
Thom, Christopher S.; Dickson, Claire F.; Gell, David A.; Weiss, Mitchell J. (March 2013). "Hemoglobin Variants: Biochemical Properties and Clinical Correlates". Cold Spring Harbor Perspectives in Medicine. 3 (3): a011858. doi:10.1101/cshperspect.a011858. ISSN 2157-1422. PMC 3579210. PMID 23388674.
Kim, Dae Sung; Baek, Hee Jo; Kim, Bo Ram; Yoon, Bo Ae; Lee, Jun Hyung; Kook, Hoon (December 2020). "The First Korean Family with Hemoglobin-M Milwaukee-2 Leading to Hereditary Methemoglobinemia". Yonsei Medical Journal. 61 (12): 1064–1067. doi:10.3349/ymj.2020.61.12.1064. ISSN 1976-2437. PMC 7700874. PMID 33251782.
Stucke, Astrid G.; Riess, Matthias L.; Connolly, Lois A. (April 2006). "Hemoglobin M (Milwaukee) affects arterial oxygen saturation and makes pulse oximetry unreliable". Anesthesiology. 104 (4): 887–888. doi:10.1097/00000542-200604000-00036. ISSN 0003-3022. PMID 16571987.

handle.net

hdl.handle.net

Iolascon, Achille; Bianchi, Paola; Andolfo, Immacolata; Russo, Roberta; Barcellini, Wilma; Fermo, Elisa; Toldi, Gergely; Ghirardello, Stefano; Rees, Davis; Van Wijk, Richard; Kattamis, Antonis (2021-09-23). "Recommendations for diagnosis and treatment of methemoglobinemia". American Journal of Hematology. 96 (12): 1666–1678. doi:10.1002/ajh.26340. hdl:1887/3249335. ISSN 0361-8609. PMC 9291883. PMID 34467556. S2CID 237377613.
Göttgens, Eva-Leonne; Baks, Kristian; Harteveld, Cornelis L.; Goossens, Kristel; van Gammeren, Adriaan J. (2021). "Cyanosis, hemolysis, decreased HbA1c and abnormal co-oximetry in a patient with hemoglobin M Saskatoon [HBB:c.190C > T p.His64Tyr]". Hematology (Amsterdam, Netherlands). 26 (1): 914–918. doi:10.1080/16078454.2021.1999048. hdl:1887/3249333. ISSN 1607-8454. PMID 34789072. S2CID 244346360.

harvard.edu

ui.adsabs.harvard.edu

Mihailescu, Mihaela-Rita; Russu, Irina M. (2001-03-27). "A signature of the T → R transition in human hemoglobin". Proceedings of the National Academy of Sciences of the United States of America. 98 (7): 3773–3777. Bibcode:2001PNAS...98.3773M. doi:10.1073/pnas.071493598. ISSN 0027-8424. PMC 31128. PMID 11259676.

karger.com

Özsoylu, S. (1972). "Congenital Methemoglobinemia Due to Hemoglobin M". Acta Haematologica. 47 (4): 225–232. doi:10.1159/000208528. ISSN 0001-5792. PMID 4625305.

nih.gov

pubmed.ncbi.nlm.nih.gov

Ludlow, John T.; Wilkerson, Richard G.; Nappe, Thomas M. (2022), "Methemoglobinemia", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30726002, retrieved 2022-03-28
Alonso-Ojembarrena, A. (2016). "Hemoglobin M Disease as a Cause of Cyanosis in a Newborn". Journal of Pediatric Hematology/Oncology. 38 (3): 173–175. doi:10.1097/MPH.0000000000000489. PMID 26694193. S2CID 26848356 – via PubMed.
Iolascon, Achille; Bianchi, Paola; Andolfo, Immacolata; Russo, Roberta; Barcellini, Wilma; Fermo, Elisa; Toldi, Gergely; Ghirardello, Stefano; Rees, Davis; Van Wijk, Richard; Kattamis, Antonis (2021-09-23). "Recommendations for diagnosis and treatment of methemoglobinemia". American Journal of Hematology. 96 (12): 1666–1678. doi:10.1002/ajh.26340. hdl:1887/3249335. ISSN 0361-8609. PMC 9291883. PMID 34467556. S2CID 237377613.
Picca, Andrew; Ruthford, Mason; Ghanim, Majd T.; Sims, Morgan; Kanter, Julie (2019-08-20). "Diagnosis of Hemoglobin M Disease in a Toddler Presenting With Hypoxemia and Hemolysis". Clinical Pediatrics. 58 (11–12): 1345–1348. doi:10.1177/0009922819870555. ISSN 0009-9228. PMID 31431070. S2CID 201115221.
Sangkitporn, S. K.; Eksiri, L.; Sangnoi, A.; Duangruang, S.; Dumbua, A.; Rattanakittisophon, K.; Sangkitporn, S. (2009). "Identification of beta-globin gene mutations in Thailand using an automated fluorescence-based DNA sequencer". International Journal of Laboratory Hematology. 31 (5): 521–527. doi:10.1111/j.1751-553X.2008.01072.x. ISSN 1751-553X. PMID 18498386. S2CID 31589532.
Rehman, Habib Ur (2001). "Methemoglobinemia". Western Journal of Medicine. 175 (3): 193–196. doi:10.1136/ewjm.175.3.193. ISSN 0093-0415. PMC 1071541. PMID 11527852.
Patnaik, Sibabratta; Natarajan, Manivachagan Muthappa; James, Ebor Jacob; Ebenezer, Kala (2014). "Methylene blue unresponsive methemoglobinemia". Indian Journal of Critical Care Medicine. 18 (4): 253–255. doi:10.4103/0972-5229.130582. ISSN 0972-5229. PMC 4033863. PMID 24872659.
Göttgens, Eva-Leonne; Baks, Kristian; Harteveld, Cornelis L.; Goossens, Kristel; van Gammeren, Adriaan J. (2021). "Cyanosis, hemolysis, decreased HbA1c and abnormal co-oximetry in a patient with hemoglobin M Saskatoon [HBB:c.190C > T p.His64Tyr]". Hematology (Amsterdam, Netherlands). 26 (1): 914–918. doi:10.1080/16078454.2021.1999048. hdl:1887/3249333. ISSN 1607-8454. PMID 34789072. S2CID 244346360.
Percy, Melanie J.; Lappin, Terry R. (2008). "Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency". British Journal of Haematology. 141 (3): 298–308. doi:10.1111/j.1365-2141.2008.07017.x. ISSN 1365-2141. PMID 18318771. S2CID 36408296.
Özsoylu, S. (1972). "Congenital Methemoglobinemia Due to Hemoglobin M". Acta Haematologica. 47 (4): 225–232. doi:10.1159/000208528. ISSN 0001-5792. PMID 4625305.
Rangan, Aruna; Savedra, Michelle E.; Dergam-Larson, Camila; Swanson, Kenneth C.; Szuberski, Jessica; Go, Ronald S.; Porter, Tavanna R.; Brunker, Sarah E.; Shi, Min; Nguyen, Phuong L.; Hoyer, James D. (August 2021). "Interpreting sulfhemoglobin and methemoglobin in patients with cyanosis: An overview of patients with M-hemoglobin variants". International Journal of Laboratory Hematology. 43 (4): 837–844. doi:10.1111/ijlh.13581. ISSN 1751-553X. PMID 34092029. S2CID 235362094.
Pisciotta, A. V.; Ebbe, S. N.; Hinz, J. E. (July 1959). "Clinical and laboratory features of two variants of methemoglobin M disease". The Journal of Laboratory and Clinical Medicine. 54 (1): 73–87. ISSN 0022-2143. PMID 13665153.
Rastogi, Loveena; Langer, Sabina; Radhakrishnan, Nita; Saxena, Renu; Kotwal, Jyoti (2020-09-30). "Hb-M Hyde Park: a rare cause of cyanosis arising from a de novo mutation". Blood Research. 55 (3): 177–180. doi:10.5045/br.2020.2020084. ISSN 2287-979X. PMC 7536569. PMID 32747614.
Spears, Frances; Banerjee, Arnab (June 2008). "Hemoglobin M variant and congenital methemoglobinemia: methylene blue will not be effective in the presence of hemoglobin M". Canadian Journal of Anaesthesia. 55 (6): 391–392. doi:10.1007/BF03021499. ISSN 0832-610X. PMID 18566207. S2CID 46308991.
Vichinsky, E. P.; Lubin, B. H. (May 1980). "Unstable hemoglobins, hemoglobins with altered oxygen affinity, and m-hemoglobins". Pediatric Clinics of North America. 27 (2): 421–428. doi:10.1016/s0031-3955(16)33859-7. ISSN 0031-3955. PMID 7383714.
Mihailescu, Mihaela-Rita; Russu, Irina M. (2001-03-27). "A signature of the T → R transition in human hemoglobin". Proceedings of the National Academy of Sciences of the United States of America. 98 (7): 3773–3777. Bibcode:2001PNAS...98.3773M. doi:10.1073/pnas.071493598. ISSN 0027-8424. PMC 31128. PMID 11259676.
Thom, Christopher S.; Dickson, Claire F.; Gell, David A.; Weiss, Mitchell J. (March 2013). "Hemoglobin Variants: Biochemical Properties and Clinical Correlates". Cold Spring Harbor Perspectives in Medicine. 3 (3): a011858. doi:10.1101/cshperspect.a011858. ISSN 2157-1422. PMC 3579210. PMID 23388674.
Kim, Dae Sung; Baek, Hee Jo; Kim, Bo Ram; Yoon, Bo Ae; Lee, Jun Hyung; Kook, Hoon (December 2020). "The First Korean Family with Hemoglobin-M Milwaukee-2 Leading to Hereditary Methemoglobinemia". Yonsei Medical Journal. 61 (12): 1064–1067. doi:10.3349/ymj.2020.61.12.1064. ISSN 1976-2437. PMC 7700874. PMID 33251782.
Stucke, Astrid G.; Riess, Matthias L.; Connolly, Lois A. (April 2006). "Hemoglobin M (Milwaukee) affects arterial oxygen saturation and makes pulse oximetry unreliable". Anesthesiology. 104 (4): 887–888. doi:10.1097/00000542-200604000-00036. ISSN 0003-3022. PMID 16571987.

ncbi.nlm.nih.gov

"Hemoglobin M disease (Concept Id: C3665425) – MedGen – NCBI". www.ncbi.nlm.nih.gov. Retrieved 2022-03-28.
Ludlow, John T.; Wilkerson, Richard G.; Nappe, Thomas M. (2022), "Methemoglobinemia", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30726002, retrieved 2022-03-28
Iolascon, Achille; Bianchi, Paola; Andolfo, Immacolata; Russo, Roberta; Barcellini, Wilma; Fermo, Elisa; Toldi, Gergely; Ghirardello, Stefano; Rees, Davis; Van Wijk, Richard; Kattamis, Antonis (2021-09-23). "Recommendations for diagnosis and treatment of methemoglobinemia". American Journal of Hematology. 96 (12): 1666–1678. doi:10.1002/ajh.26340. hdl:1887/3249335. ISSN 0361-8609. PMC 9291883. PMID 34467556. S2CID 237377613.
Rehman, Habib Ur (2001). "Methemoglobinemia". Western Journal of Medicine. 175 (3): 193–196. doi:10.1136/ewjm.175.3.193. ISSN 0093-0415. PMC 1071541. PMID 11527852.
Patnaik, Sibabratta; Natarajan, Manivachagan Muthappa; James, Ebor Jacob; Ebenezer, Kala (2014). "Methylene blue unresponsive methemoglobinemia". Indian Journal of Critical Care Medicine. 18 (4): 253–255. doi:10.4103/0972-5229.130582. ISSN 0972-5229. PMC 4033863. PMID 24872659.
Rastogi, Loveena; Langer, Sabina; Radhakrishnan, Nita; Saxena, Renu; Kotwal, Jyoti (2020-09-30). "Hb-M Hyde Park: a rare cause of cyanosis arising from a de novo mutation". Blood Research. 55 (3): 177–180. doi:10.5045/br.2020.2020084. ISSN 2287-979X. PMC 7536569. PMID 32747614.
Mihailescu, Mihaela-Rita; Russu, Irina M. (2001-03-27). "A signature of the T → R transition in human hemoglobin". Proceedings of the National Academy of Sciences of the United States of America. 98 (7): 3773–3777. Bibcode:2001PNAS...98.3773M. doi:10.1073/pnas.071493598. ISSN 0027-8424. PMC 31128. PMID 11259676.
Thom, Christopher S.; Dickson, Claire F.; Gell, David A.; Weiss, Mitchell J. (March 2013). "Hemoglobin Variants: Biochemical Properties and Clinical Correlates". Cold Spring Harbor Perspectives in Medicine. 3 (3): a011858. doi:10.1101/cshperspect.a011858. ISSN 2157-1422. PMC 3579210. PMID 23388674.
Kim, Dae Sung; Baek, Hee Jo; Kim, Bo Ram; Yoon, Bo Ae; Lee, Jun Hyung; Kook, Hoon (December 2020). "The First Korean Family with Hemoglobin-M Milwaukee-2 Leading to Hereditary Methemoglobinemia". Yonsei Medical Journal. 61 (12): 1064–1067. doi:10.3349/ymj.2020.61.12.1064. ISSN 1976-2437. PMC 7700874. PMID 33251782.

sagepub.com

journals.sagepub.com

Picca, Andrew; Ruthford, Mason; Ghanim, Majd T.; Sims, Morgan; Kanter, Julie (2019-08-20). "Diagnosis of Hemoglobin M Disease in a Toddler Presenting With Hypoxemia and Hemolysis". Clinical Pediatrics. 58 (11–12): 1345–1348. doi:10.1177/0009922819870555. ISSN 0009-9228. PMID 31431070. S2CID 201115221.

sciencedirect.com

Randolph, Tim R. (2020-01-01), Keohane, Elaine M.; Otto, Catherine N.; Walenga, Jeanine M. (eds.), "24 - Hemoglobinopathies (structural defects in hemoglobin)", Rodak's Hematology (Sixth Edition), St. Louis (MO): Elsevier, pp. 394–423, ISBN 978-0-323-53045-3, retrieved 2022-03-28
Leung, Kwok Yin; Au, Patrick; Tang, Mary (2020-01-01), Pandya, Pranav P.; Oepkes, Dick; Sebire, Neil J.; Wapner, Ronald J. (eds.), "27 - Prenatal Screening for Thalassemias", Fetal Medicine (Third Edition), London: Elsevier, pp. 263–273.e1, ISBN 978-0-7020-6956-7, retrieved 2022-03-28
Old, John (2013-01-01), Rimoin, David; Pyeritz, Reed; Korf, Bruce (eds.), "Chapter 71 - Hemoglobinopathies and Thalassemias", Emery and Rimoin's Principles and Practice of Medical Genetics (Sixth Edition), Oxford: Academic Press, pp. 1–44, ISBN 978-0-12-383834-6, retrieved 2022-03-28

semanticscholar.org

api.semanticscholar.org

Alonso-Ojembarrena, A. (2016). "Hemoglobin M Disease as a Cause of Cyanosis in a Newborn". Journal of Pediatric Hematology/Oncology. 38 (3): 173–175. doi:10.1097/MPH.0000000000000489. PMID 26694193. S2CID 26848356 – via PubMed.
Iolascon, Achille; Bianchi, Paola; Andolfo, Immacolata; Russo, Roberta; Barcellini, Wilma; Fermo, Elisa; Toldi, Gergely; Ghirardello, Stefano; Rees, Davis; Van Wijk, Richard; Kattamis, Antonis (2021-09-23). "Recommendations for diagnosis and treatment of methemoglobinemia". American Journal of Hematology. 96 (12): 1666–1678. doi:10.1002/ajh.26340. hdl:1887/3249335. ISSN 0361-8609. PMC 9291883. PMID 34467556. S2CID 237377613.
Picca, Andrew; Ruthford, Mason; Ghanim, Majd T.; Sims, Morgan; Kanter, Julie (2019-08-20). "Diagnosis of Hemoglobin M Disease in a Toddler Presenting With Hypoxemia and Hemolysis". Clinical Pediatrics. 58 (11–12): 1345–1348. doi:10.1177/0009922819870555. ISSN 0009-9228. PMID 31431070. S2CID 201115221.
Sangkitporn, S. K.; Eksiri, L.; Sangnoi, A.; Duangruang, S.; Dumbua, A.; Rattanakittisophon, K.; Sangkitporn, S. (2009). "Identification of beta-globin gene mutations in Thailand using an automated fluorescence-based DNA sequencer". International Journal of Laboratory Hematology. 31 (5): 521–527. doi:10.1111/j.1751-553X.2008.01072.x. ISSN 1751-553X. PMID 18498386. S2CID 31589532.
Göttgens, Eva-Leonne; Baks, Kristian; Harteveld, Cornelis L.; Goossens, Kristel; van Gammeren, Adriaan J. (2021). "Cyanosis, hemolysis, decreased HbA1c and abnormal co-oximetry in a patient with hemoglobin M Saskatoon [HBB:c.190C > T p.His64Tyr]". Hematology (Amsterdam, Netherlands). 26 (1): 914–918. doi:10.1080/16078454.2021.1999048. hdl:1887/3249333. ISSN 1607-8454. PMID 34789072. S2CID 244346360.
Percy, Melanie J.; Lappin, Terry R. (2008). "Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency". British Journal of Haematology. 141 (3): 298–308. doi:10.1111/j.1365-2141.2008.07017.x. ISSN 1365-2141. PMID 18318771. S2CID 36408296.
Rangan, Aruna; Savedra, Michelle E.; Dergam-Larson, Camila; Swanson, Kenneth C.; Szuberski, Jessica; Go, Ronald S.; Porter, Tavanna R.; Brunker, Sarah E.; Shi, Min; Nguyen, Phuong L.; Hoyer, James D. (August 2021). "Interpreting sulfhemoglobin and methemoglobin in patients with cyanosis: An overview of patients with M-hemoglobin variants". International Journal of Laboratory Hematology. 43 (4): 837–844. doi:10.1111/ijlh.13581. ISSN 1751-553X. PMID 34092029. S2CID 235362094.
Spears, Frances; Banerjee, Arnab (June 2008). "Hemoglobin M variant and congenital methemoglobinemia: methylene blue will not be effective in the presence of hemoglobin M". Canadian Journal of Anaesthesia. 55 (6): 391–392. doi:10.1007/BF03021499. ISSN 0832-610X. PMID 18566207. S2CID 46308991.

wiley.com

onlinelibrary.wiley.com

Arceci, Robert J.; Hann, Ian M.; Smith, Owen P., eds. (2006-08-31). Pediatric Hematology. Blackwell Publishing. doi:10.1002/9780470987001. ISBN 9780470987001.

worldcat.org

search.worldcat.org

Iolascon, Achille; Bianchi, Paola; Andolfo, Immacolata; Russo, Roberta; Barcellini, Wilma; Fermo, Elisa; Toldi, Gergely; Ghirardello, Stefano; Rees, Davis; Van Wijk, Richard; Kattamis, Antonis (2021-09-23). "Recommendations for diagnosis and treatment of methemoglobinemia". American Journal of Hematology. 96 (12): 1666–1678. doi:10.1002/ajh.26340. hdl:1887/3249335. ISSN 0361-8609. PMC 9291883. PMID 34467556. S2CID 237377613.
Picca, Andrew; Ruthford, Mason; Ghanim, Majd T.; Sims, Morgan; Kanter, Julie (2019-08-20). "Diagnosis of Hemoglobin M Disease in a Toddler Presenting With Hypoxemia and Hemolysis". Clinical Pediatrics. 58 (11–12): 1345–1348. doi:10.1177/0009922819870555. ISSN 0009-9228. PMID 31431070. S2CID 201115221.
Sangkitporn, S. K.; Eksiri, L.; Sangnoi, A.; Duangruang, S.; Dumbua, A.; Rattanakittisophon, K.; Sangkitporn, S. (2009). "Identification of beta-globin gene mutations in Thailand using an automated fluorescence-based DNA sequencer". International Journal of Laboratory Hematology. 31 (5): 521–527. doi:10.1111/j.1751-553X.2008.01072.x. ISSN 1751-553X. PMID 18498386. S2CID 31589532.
Rehman, Habib Ur (2001). "Methemoglobinemia". Western Journal of Medicine. 175 (3): 193–196. doi:10.1136/ewjm.175.3.193. ISSN 0093-0415. PMC 1071541. PMID 11527852.
Patnaik, Sibabratta; Natarajan, Manivachagan Muthappa; James, Ebor Jacob; Ebenezer, Kala (2014). "Methylene blue unresponsive methemoglobinemia". Indian Journal of Critical Care Medicine. 18 (4): 253–255. doi:10.4103/0972-5229.130582. ISSN 0972-5229. PMC 4033863. PMID 24872659.
Göttgens, Eva-Leonne; Baks, Kristian; Harteveld, Cornelis L.; Goossens, Kristel; van Gammeren, Adriaan J. (2021). "Cyanosis, hemolysis, decreased HbA1c and abnormal co-oximetry in a patient with hemoglobin M Saskatoon [HBB:c.190C > T p.His64Tyr]". Hematology (Amsterdam, Netherlands). 26 (1): 914–918. doi:10.1080/16078454.2021.1999048. hdl:1887/3249333. ISSN 1607-8454. PMID 34789072. S2CID 244346360.
Percy, Melanie J.; Lappin, Terry R. (2008). "Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency". British Journal of Haematology. 141 (3): 298–308. doi:10.1111/j.1365-2141.2008.07017.x. ISSN 1365-2141. PMID 18318771. S2CID 36408296.
Özsoylu, S. (1972). "Congenital Methemoglobinemia Due to Hemoglobin M". Acta Haematologica. 47 (4): 225–232. doi:10.1159/000208528. ISSN 0001-5792. PMID 4625305.
Rangan, Aruna; Savedra, Michelle E.; Dergam-Larson, Camila; Swanson, Kenneth C.; Szuberski, Jessica; Go, Ronald S.; Porter, Tavanna R.; Brunker, Sarah E.; Shi, Min; Nguyen, Phuong L.; Hoyer, James D. (August 2021). "Interpreting sulfhemoglobin and methemoglobin in patients with cyanosis: An overview of patients with M-hemoglobin variants". International Journal of Laboratory Hematology. 43 (4): 837–844. doi:10.1111/ijlh.13581. ISSN 1751-553X. PMID 34092029. S2CID 235362094.
Pisciotta, A. V.; Ebbe, S. N.; Hinz, J. E. (July 1959). "Clinical and laboratory features of two variants of methemoglobin M disease". The Journal of Laboratory and Clinical Medicine. 54 (1): 73–87. ISSN 0022-2143. PMID 13665153.
Rastogi, Loveena; Langer, Sabina; Radhakrishnan, Nita; Saxena, Renu; Kotwal, Jyoti (2020-09-30). "Hb-M Hyde Park: a rare cause of cyanosis arising from a de novo mutation". Blood Research. 55 (3): 177–180. doi:10.5045/br.2020.2020084. ISSN 2287-979X. PMC 7536569. PMID 32747614.
Nelson textbook of pediatrics. Robert Kliegman, Bonita Stanton, Joseph W., III St. Geme, Nina Felice Schor, Richard E. Behrman, Waldo E. Preceded by: Nelson (Edition 21 ed.). Philadelphia, PA. 2020. ISBN 978-0-323-56888-3. OCLC 1096283151.{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: others (link)
Spears, Frances; Banerjee, Arnab (June 2008). "Hemoglobin M variant and congenital methemoglobinemia: methylene blue will not be effective in the presence of hemoglobin M". Canadian Journal of Anaesthesia. 55 (6): 391–392. doi:10.1007/BF03021499. ISSN 0832-610X. PMID 18566207. S2CID 46308991.
Vichinsky, E. P.; Lubin, B. H. (May 1980). "Unstable hemoglobins, hemoglobins with altered oxygen affinity, and m-hemoglobins". Pediatric Clinics of North America. 27 (2): 421–428. doi:10.1016/s0031-3955(16)33859-7. ISSN 0031-3955. PMID 7383714.
Nathan and Oski's hematology and oncology of infancy and childhood. Stuart H. Orkin, David E. Fisher, David Ginsburg, A. Thomas Look, Samuel E. Lux, David G. Nathan (8th ed.). Philadelphia, PA. 2015. ISBN 978-0-323-29177-4. OCLC 894113533.{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: others (link)
Mihailescu, Mihaela-Rita; Russu, Irina M. (2001-03-27). "A signature of the T → R transition in human hemoglobin". Proceedings of the National Academy of Sciences of the United States of America. 98 (7): 3773–3777. Bibcode:2001PNAS...98.3773M. doi:10.1073/pnas.071493598. ISSN 0027-8424. PMC 31128. PMID 11259676.
Thom, Christopher S.; Dickson, Claire F.; Gell, David A.; Weiss, Mitchell J. (March 2013). "Hemoglobin Variants: Biochemical Properties and Clinical Correlates". Cold Spring Harbor Perspectives in Medicine. 3 (3): a011858. doi:10.1101/cshperspect.a011858. ISSN 2157-1422. PMC 3579210. PMID 23388674.
Kim, Dae Sung; Baek, Hee Jo; Kim, Bo Ram; Yoon, Bo Ae; Lee, Jun Hyung; Kook, Hoon (December 2020). "The First Korean Family with Hemoglobin-M Milwaukee-2 Leading to Hereditary Methemoglobinemia". Yonsei Medical Journal. 61 (12): 1064–1067. doi:10.3349/ymj.2020.61.12.1064. ISSN 1976-2437. PMC 7700874. PMID 33251782.
Stucke, Astrid G.; Riess, Matthias L.; Connolly, Lois A. (April 2006). "Hemoglobin M (Milwaukee) affects arterial oxygen saturation and makes pulse oximetry unreliable". Anesthesiology. 104 (4): 887–888. doi:10.1097/00000542-200604000-00036. ISSN 0003-3022. PMID 16571987.

worldcat.org

Nelson textbook of pediatrics. Robert Kliegman, Bonita Stanton, Joseph W., III St. Geme, Nina Felice Schor, Richard E. Behrman, Waldo E. Preceded by: Nelson (Edition 21 ed.). Philadelphia, PA. 2020. ISBN 978-0-323-56888-3. OCLC 1096283151.{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: others (link)
Nathan and Oski's hematology and oncology of infancy and childhood. Stuart H. Orkin, David E. Fisher, David Ginsburg, A. Thomas Look, Samuel E. Lux, David G. Nathan (8th ed.). Philadelphia, PA. 2015. ISBN 978-0-323-29177-4. OCLC 894113533.{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: others (link)