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Journal articles on the topic 'Hematologiese'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Delforge, Michel. "Being a hematologist." International Journal of Hematologic Oncology 3, no. 4 (2014): 249–51. http://dx.doi.org/10.2217/ijh.14.29.

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2

Kaspers, G. J. L. "Kinderoncologie/hematologie VUmc." Tijdschrift voor Kindergeneeskunde 81, S1 (2013): 182–86. http://dx.doi.org/10.1007/s12456-013-0142-7.

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3

Iancu, Mihaela Adela, Mihaela Daniela Baltă, Cristian Gabriel Bejan, Alexandra Ana Maria Stănescu, Dumitru Matei, and Camelia Cristina Diaconu. "Hematological manifestations in intestinal inflammatory diseases." Romanian Medical Journal 65, no. 2 (2018): 108–11. http://dx.doi.org/10.37897/rmj.2018.2.6.

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4

WILHELM, MORTON C., ROBERT E. JONES, READ McGEHEE, JAMES S. MITCHENER, WILLIAM R. SANDUSKY, and CHARLES E. HESS. "Splenectomy in Hematologie Disorders." Annals of Surgery 207, no. 5 (1988): 581–89. http://dx.doi.org/10.1097/00000658-198805000-00012.

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5

Berentsen, Sigbjørn. "Nevropsykiatrisk sykdom med hematologiske funn." Tidsskrift for Den norske legeforening 129, no. 1 (2009): 35. http://dx.doi.org/10.4045/tidsskr.2009.0121.

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6

Harris, J. W. "PARVOVIRUS B19 FOR THE HEMATOLOGIST." Pediatric Infectious Disease Journal 11, no. 9 (1992): 784. http://dx.doi.org/10.1097/00006454-199209000-00036.

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7

Harris, John W. "Parvovirus B19 for the hematologist." American Journal of Hematology 39, no. 2 (1992): 119–30. http://dx.doi.org/10.1002/ajh.2830390209.

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8

Dainiak, Nicholas, Jamie K. Waselenko, James O. Armitage, Thomas J. MacVittie, and Ann M. Farese. "The Hematologist and Radiation Casualties." Hematology 2003, no. 1 (2003): 473–96. http://dx.doi.org/10.1182/asheducation-2003.1.473.

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Abstract Since the terrorist attack of September 11, 2001, preparation by the health care system for an act of terrorism has been mandated by leaders of governments. Scenarios for terrorist acts involving radioactive material have been identified, and approaches to management (based on past experience from atomic weapons detonations and radiation accidents) have been developed. Because of their experience in managing patients with profound cytopenia and/or marrow aplasia, hematologists will be asked to play a significant role in evaluating and treating victims of mass accidental or deliberate

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9

Luciani, A., F. Pigneur, P. Beaussart, and A. Rahmouni. "Hematologie : applications IRM corps entier." Journal de Radiologie 90, no. 10 (2009): 1338. http://dx.doi.org/10.1016/s0221-0363(09)75314-4.

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10

Drochioi, Ana Simona, Evelina Moraru, Bogdan Diaconu, and Dan Cristian Moraru. "Hematological aspects in viral hepatitis C in children." Romanian Medical Journal 65, no. 3 (2018): 196–201. http://dx.doi.org/10.37897/rmj.2018.3.7.

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11

Nica, Adriana, Ana Maria Vlădăreanu, Ion Dumitru, and Minodora Onisâi. "Splenectomy – diagnostic and therapeutic option in haematological disorders." Romanian Medical Journal 62, no. 1 (2015): 30–34. http://dx.doi.org/10.37897/rmj.2015.1.6.

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For hematologic disorders, splenectomy has a wide range of applications: diagnosis, palliative or curative. The most frequent indication is for red cell disorders: hereditary spherocytosis, autoimmune hemolytic anemia or thalassemia. For the platelet disorders, the greatest benefit is achieved in idiopathic thrombocytopenic purpura. In case of limfoproliferative disorders (leukemia, lymphoma), splenectomy plays a role in diagnosis, palliative care (lowering of tumor burden) and in some cases as a cure. In patients with hematologic disorders, splenectomy is associated with an elevated risk of i

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12

Mady, Ahmed F., Basim R. Huwait, Muhammad Asim Rana, Omar E. Ramadan, Abulrahman Al-Harthy, and Abdul Kareem M. Al-Momen. "Acquired Hemophilia Network;non Hematologist Perspectives." Blood 124, no. 21 (2014): 5978. http://dx.doi.org/10.1182/blood.v124.21.5978.5978.

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Abstract Background: Acquired hemophilia (AH) is an autoimmune disease caused by an autoantibody to factor VIII (FVIII). Morbidity and mortality are high due to the age of the patients, underlying diseases, the toxic effects of immunosuppression, bleeding and is in part attributable to sequential delays in diagnosis and appropriate treatment. Objective: AH usually presents to clinicians without prior experience of the disease, therefore diagnosis is frequently delayed and bleeds under treated. Therefore improving the awareness among health care professionals to whom AH patients are likely to p

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13

Masterson, Monica, Michael Levitt, Patricia Greenberg, David B. Greenberg, and Arthur A. Topilow. "Choosing Wisely in Thrombophilia: Hematologist Required." Blood 128, no. 22 (2016): 4994. http://dx.doi.org/10.1182/blood.v128.22.4994.4994.

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Abstract Background: Selection for thrombophilia testing among patients with venous thromboembolism (VTE) is controversial. Choosing Wisely guidelines published by the American Society of Hematology (ASH) recommend against testing patients with VTE provoked by the major transient risk factors of major surgery, immobility and trauma. Testing is most often considered in patients with recurrent VTE, unprovoked VTE, VTE occurring in an unusual site, and a significant family history of VTE. The purpose of this study was to review the practices in thrombophilia testing at Jersey Shore University Med

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14

Moiz, Bushra, Zaid Muslim, Zahraa Farrukh Siddiqui, and Hasnain Zafar. "Acute Mesenteric Thrombosis: A Hematologist Perspective." Clinical and Applied Thrombosis/Hemostasis 26 (January 1, 2020): 107602962093299. http://dx.doi.org/10.1177/1076029620932999.

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15

Means, Robert T. "The Greatest Hematologist in the World." American Journal of the Medical Sciences 351, no. 3 (2016): 323–24. http://dx.doi.org/10.1016/j.amjms.2016.01.003.

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16

Kaneko, J. J. "Animal models of inherited hematologie disease." Clinica Chimica Acta 165, no. 1 (1987): 1–19. http://dx.doi.org/10.1016/0009-8981(87)90213-0.

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17

Mainous, Arch G., Benjamin Rooks, Rebecca J. Tanner, Peter J. Carek, Vandy Black, and Thomas D. Coates. "Shared Care for Adults with Sickle Cell Disease: An Analysis of Care from Eight Health Systems." Journal of Clinical Medicine 8, no. 8 (2019): 1154. http://dx.doi.org/10.3390/jcm8081154.

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Adult sickle cell disease (SCD) patients frequently transition from pediatric hematology to adult primary care. We examined healthcare utilization for adult patients with SCD with shared care between hematologists and primary care providers (PCP). We analyzed the OneFlorida Data Trust, a centralized data repository of electronic medical record (EMR) data from eight different health systems in Florida. The number of included adults with SCD was 1147. We examined frequent hospitalizations and emergency department (ED) visits by whether the patient had shared care or single specialty care alone.

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18

Hagve, Tor-Arne, Kristin Lilleholt, and Marianne Svendsen. "Jernmangelanemi - tolking av biokjemiske og hematologiske funn." Tidsskrift for Den norske legeforening 133, no. 2 (2013): 161–64. http://dx.doi.org/10.4045/tidsskr.12.0192.

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19

Kucharz, Eugene Joseph, Marc A. Shampo, and Robert A. Kyle. "Ludwik Hirszfeld—Polish Immunologist, Microbiologist, and Hematologist." Mayo Clinic Proceedings 85, no. 5 (2010): e35. http://dx.doi.org/10.4065/mcp.2010.0251.

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20

Uchiba, Mitsuhiro. "Kumamoto Earthquakes; One week of a hematologist." Japanese Journal of Thrombosis and Hemostasis 27, no. 6 (2016): 697–701. http://dx.doi.org/10.2491/jjsth.27.697.

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21

Hoban, Megan D., and Daniel E. Bauer. "A genome editing primer for the hematologist." Blood 127, no. 21 (2016): 2525–35. http://dx.doi.org/10.1182/blood-2016-01-678151.

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Abstract Gene editing enables the site-specific modification of the genome. These technologies have rapidly advanced such that they have entered common use in experimental hematology to investigate genetic function. In addition, genome editing is becoming increasingly plausible as a treatment modality to rectify genetic blood disorders and improve cellular therapies. Genome modification typically ensues from site-specific double-strand breaks and may result in a myriad of outcomes. Even single-strand nicks and targeted biochemical modifications that do not permanently alter the DNA sequence (e

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22

Johnny, Fris, Zafran Zafran, Des Roza, and Ketut Mahardika. "HEMATOLOGIS BEBERAPA SPESIES IKAN LAUT BUDI DAYA." Jurnal Penelitian Perikanan Indonesia 9, no. 4 (2017): 63. http://dx.doi.org/10.15578/jppi.9.4.2003.63-71.

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Suatu percobaan dengan tujuan mendapatkan keragaan hematologis beberapa jenis ikan laut budi daya telah dilakukan. lkan uji yang digunakan adalah ikan bandeng (Chanos chanos Forskal), kakap putih (Lafes calcarifer), napoleon (Cheilinus undulates), kerapu lumpur (Epinephelus coioides), kerapu macan (Epinephelus fuscoguttafus), dan kerapu bebek (Cromileptes altivelis).

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23

ZAUBER, N. P., and A. G. ZAUBER. "Hematologie Data of Healthy Very Old People." Survey of Anesthesiology 32, no. 1 (1988): 9. http://dx.doi.org/10.1097/00132586-198802000-00010.

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24

Kapoor, Prashant, Jonas Paludo, Nishanth Vallumsetla, and Philip R. Greipp. "Waldenström macroglobulinemia: What a hematologist needs to know." Blood Reviews 29, no. 5 (2015): 301–19. http://dx.doi.org/10.1016/j.blre.2015.03.001.

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25

Abuhadra, Nour, Navneet S. Majhail, and Aziz Nazha. "Impact of social media for the hematologist/oncologist." Seminars in Hematology 54, no. 4 (2017): 193–97. http://dx.doi.org/10.1053/j.seminhematol.2017.07.003.

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26

Bonkovsky, Herbert L. "Neurovisceral Porphyrias: What a Hematologist Needs to Know." Hematology 2005, no. 1 (2005): 24–30. http://dx.doi.org/10.1182/asheducation-2005.1.24.

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Abstract The acute or inducible hepatic porphyrias comprise four inherited disorders of heme biosynthesis. They usually remain asymptomatic for most of the lifespan of individuals who inherit the specific enzyme deficiencies but may cause life-threatening attacks of neurovisceral symptoms. Failure to consider the diagnosis frequently delays effective treatment, and inappropriate diagnostic tests and/or mistaken interpretation of results may lead to misdiagnosis and inappropriate treatment. The four disorders are ALA dehydratase deficiency porphyria, acute intermittent porphyria, hereditary cop

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27

Yuliandra, Yori, Hansen Nasif, Sabrina Ermayanti, Lilik Sulistyowati, and Dian A. Juwita. "Hematologic Toxicities of Chemotherapy in Lung Cancer Patients: A Retrospective Study in Dr. M. Djamil Hospital Padang, Indonesia." Indonesian Journal of Clinical Pharmacy 8, no. 2 (2019): 129. http://dx.doi.org/10.15416/ijcp.2019.8.2.129.

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The use of chemotherapeutic agents in the management of cancer is often followed by a range of toxicities to various organ systems. A retrospective study on the hematologic toxicities of chemotherapy in lung cancer patients has been carried out. The study was conducted by a cross-sectional method from medical records of four-year data in 2010–2014 at Dr. M. Djamil Hospital Padang, West Sumatra, Indonesia. Data from medical records of patients diagnosed with lung cancer and underwent chemotherapy, not suffering from primary hematologic diseases, and with normal kidney and liver function prior t

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28

Terrell, Deirdra, Laura A. Beebe, James W. Mold, James George, and Sara K. Vesely. "What Level of Platelet Count and Symptoms Trigger Referral of Patients with Thrombocytopenia from Primary Care Physicians to Hematologists?" Blood 112, no. 11 (2008): 4692. http://dx.doi.org/10.1182/blood.v112.11.4692.4692.

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Abstract Introduction : Primary care physicians are typically the first physicians who see patients with thrombocytopenia. There are currently no data to document which patients who present with isolated thrombocytopenia or immune thrombocytopenic purpura (ITP) are referred to hematologists. The published ASH Practice Guideline on ITP (Blood1996;88:3) does not address the issue of referral to a hematologist; the British Committee for Standards in Haematology Guideline on ITP (Brit J Haematol2003;120:574) only recommends referral of children with severe chronic ITP. The goal of this study was t

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29

Kreidieh, Firas, and Sally Temraz. "SARS-CoV-2 INFECTED PATIENTS: FROM A HEMATOLOGIST PERSPECTIVE." Mediterranean Journal of Hematology and Infectious Diseases 12, no. 1 (2020): e2020078. http://dx.doi.org/10.4084/mjhid.2020.078.

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Introduction: According to the World Health Organization (WHO), COVID-19 has become a Public Health Emergency of International Concern (PHEIC). Understanding the hematologic findings of patients with SARS-CoV-2 infection is essential to promote their care and improve outcomes.  Objective:In this review, we aim at summarizing changes in the hematopoietic system and hemostasis that occur in SARS-CoV-2 infected patients.  Findings: COVID-19 infection is often associated with laboratory hematologic findings that can have important clinical implications. Careful revision of

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30

Lecompte, T. P. "Antithrombotic agents and invasive procedures - Hematologist point of view." Thrombosis Research 130 (October 2012): S61—S62. http://dx.doi.org/10.1016/j.thromres.2012.08.278.

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31

Chen, Luke Y. C., Andre Mattman, Michael A. Seidman, and Mollie N. Carruthers. "IgG4-related disease: what a hematologist needs to know." Haematologica 104, no. 3 (2019): 444–55. http://dx.doi.org/10.3324/haematol.2018.205526.

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32

Tao, Derrick L., Aaron Boothby, Joel McLouth, and Vinay Prasad. "Financial Conflicts of Interest Among Hematologist-Oncologists on Twitter." JAMA Internal Medicine 177, no. 3 (2017): 425. http://dx.doi.org/10.1001/jamainternmed.2016.8467.

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33

Patrick, Cory, Kaitlin McIntyre, Rakesh Singal, and Damien Mikael Hansra. "Evaluation of patient's versus hematologist/oncologist's office visit agenda." Journal of Clinical Oncology 34, no. 26_suppl (2016): 125. http://dx.doi.org/10.1200/jco.2016.34.26_suppl.125.

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125 Background: Few studies have been reported in oncology regarding elements of physician agenda. We aim to compare elements of a doctor office visit agenda between hem/onc physicians (MD) and patients (pts). Methods: Pts and MDs were enrolled to completed a five question survey. Pts were asked: “My doctor” Focuses more on quantity of life and less on quality of life, spends enough time with me, addresses symptoms, addresses chemo side effects, and addresses prognosis. MDs were asked the same questions but worded: "I” spend enough time with pts for example. Answers were recorded on a 5 point

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34

Oo, Thein H. "Pattern of Consultation Referrals for Cytopenia Evaluations to a Hematologist at An Academic Medical Center: The Expanding Role of a Consultant Hematologist." Blood 112, no. 11 (2008): 4673. http://dx.doi.org/10.1182/blood.v112.11.4673.4673.

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Abstract Purpose: It appears that many cytopenia consultation referrals to Hematology outpatient clinics turn out to have diseases related to primary care practice. The aim of this retrospective study is to see what proportion and what kind of cytopenia consultations in a Hematology clinic are due to disorders related to primary care practice. Methods: Retrospective chart review analysis of all outpatient referrals from July 2002 to June 2008 to a Hematologist at a tertiary university hospital was performed. Of those, only cytopenia consultations were analyzed. Cases were analyzed according to

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35

Zainun, Zakki. "PENGAMATAN PARAMETER HEMATOLOGIS PADA IKAN MAS YANG DIBERI IMMUNOSTIMULAN." Buletin Teknik Litkayasa Akuakultur 6, no. 1 (2017): 45. http://dx.doi.org/10.15578/blta.6.1.2007.45-49.

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Darah mempunyai peran fisiologis penting pada ikan, penyimpangan hematologis dan respon kebal ikan mencirikan terjadinya perubahan status kesehatan ikan dari kondisi normal menjadi abnormal. Perubahan gambaran darah dapat menentukan kondisi ikan atau status kesehatannya. Pengamatan parameter darah dilakukan pada ikan mas yang telah diberi imunostimulan dan kontrol. Pengambilan sampel darah dilakukan pada hari ke-0, 7, 14, 21, dan 28. Parameter yang diamati adalah indeks fagositik, total leukosit, dan hematokrit. Hasil pengamatan indeks fagositik menunjukkan bahwa terjadi peningkatan kekebalan

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36

Herbrecht, R., K. L. Liu, Y. Fuhrer, F. Jehl, and F. Oberling. "Les infections a staphylocoques a coagulase negative en hematologie." Médecine et Maladies Infectieuses 20 (March 1990): 103–8. http://dx.doi.org/10.1016/s0399-077x(05)81097-2.

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37

Tendas, Andrea, Pasquale Niscola, Laura Scaramucci, et al. "Dysgeusia in patients with hematological malignancies: a reminder for hematologist." Journal of Oral Pathology & Medicine 42, no. 4 (2012): 352–53. http://dx.doi.org/10.1111/jop.12034.

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38

Luban, Naomi L. C., Eileen McBride, Jason C. Ford, and Sumit Gupta. "Transfusion medicine problems and solutions for the pediatric hematologist/oncologist." Pediatric Blood & Cancer 58, no. 7 (2012): 1106–11. http://dx.doi.org/10.1002/pbc.24077.

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39

Kreuziger, Lisa Baumann, and M. Patricia Massicotte. "Adult and pediatric mechanical circulation: a guide for the hematologist." Hematology 2018, no. 1 (2018): 507–15. http://dx.doi.org/10.1182/asheducation-2018.1.507.

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Abstract Mechanical circulatory support (MCS) is the overarching term that encompasses the temporary and durable devices used in patients with severe heart failure. MCS disturbs the hematologic and coagulation system, leading to platelet activation, activation of the contact pathway of coagulation, and acquired von Willebrand syndrome. Ischemic stroke and major hemorrhage occur in up to 30% of patients. Hematologists are an essential part of the MCS team because they understand the delicate balance between bleeding and clotting and alteration of hemostasis with antithrombotic therapy. However,

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40

Green, Ralph. "Vitamin B12 deficiency from the perspective of a practicing hematologist." Blood 129, no. 19 (2017): 2603–11. http://dx.doi.org/10.1182/blood-2016-10-569186.

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AbstractB12 deficiency is the leading cause of megaloblastic anemia, and although more common in the elderly, can occur at any age. Clinical disease caused by B12 deficiency usually connotes severe deficiency, resulting from a failure of the gastric or ileal phase of physiological B12 absorption, best exemplified by the autoimmune disease pernicious anemia. There are many other causes of B12 deficiency, which range from severe to mild. Mild deficiency usually results from failure to render food B12 bioavailable or from dietary inadequacy. Although rarely resulting in megaloblastic anemia, mild

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41

Martins, José Murilo. "Universal iron fortification of foods: the view of a hematologist." Revista Brasileira de Hematologia e Hemoterapia 34, no. 6 (2012): 459–63. http://dx.doi.org/10.5581/1516-8484.20120113.

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42

Buyukkurt, Nurhilal, Funda Tanrikulu, Suheyl Asma, and Hakan Ozdogu. "Final diagnosis of patients referred to hematologist due to anemia." Medicine Science | International Medical Journal 9, no. 1 (2020): 1. http://dx.doi.org/10.5455/medscience.2019.08.9156.

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43

Torres, Rodrigo Martín, and Pablo Gabriel Lódolo. "Red eyes first sign of the sickle cell disease." Optometry Reports 1, no. 1 (2011): 1. http://dx.doi.org/10.4081/optometry.2011.e1.

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A patient with red eyes and ocular decongestants drops (tetrahidrozolyne 0.05%) use history, was observed by an optometrist and referred to an ophthalmic consult. The redness of their eyes was secondary to conjunctival vessel micro-hemorraghe (petechiaes). After a complete ophthalmology and hematologist exploration a Cell Sickle Disease was diagnosed as the cause of the vascular disorder. An hematologist treat it and the ocular redness was resolved. This case emphasizes the problem about self-medication and remark the importance of the optometrist working together with the ophthalmologist to p

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44

Neier, Michelle, Michele P. Lambert, Rachael F. Grace, et al. "The Effect of "Pathway" to Diagnosis for Childhood ITP on Caregiver Quality of Life at Time of Diagnosis." Blood 134, Supplement_1 (2019): 2174. http://dx.doi.org/10.1182/blood-2019-125686.

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Background: Immune thrombocytopenia (ITP) is an immune mediated bleeding disorder characterized by isolated thrombocytopenia. ITP can have a variety of presentations from asymptomatic to life threatening bleeding. Although childhood ITP is most often a self-resolving illness which can be closely observed without intervention, it can be associated with significant impact on quality of life (QoL). Prospective studies of QoL in ITP patients show that there is not always a correlation with treatment or disease severity. The pathway from initial presentation to final diagnosis varies and may includ

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45

Wildes, Tanya M., and Kenneth C. Anderson. "Approach to the treatment of the older, unfit patient with myeloma from diagnosis to relapse: perspectives of a US hematologist and a geriatric hematologist." Hematology 2018, no. 1 (2018): 88–96. http://dx.doi.org/10.1182/asheducation-2018.1.88.

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Abstract Mrs. A. is a 73-year-old woman who has developed increasing fatigue and lower back pain over the past year. The pain limits her exercise tolerance such that she can now walk only 1 block. She is a retired schoolteacher who does volunteer efforts in her community but has limited her activities due to fatigue. Karnofsky performance status is 70%. She has a history of chronic hypertension treated with a diuretic, adult-onset diabetes mellitus treated with metformin, and hypothyroidism treated with levothyroxine. Initial evaluation reveals anemia, renal dysfunction, an elevated total prot

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46

Ravindran, Aishwarya, Wilson I. Gonsalves, Shahrukh K. Hashmi, et al. "Estimating the Annual Volume of Hematologic Cancer Cases per Hematologist-Oncologist in the United States: Are We Treating Rare Cancers Too Rarely?" Blood 126, no. 23 (2015): 3297. http://dx.doi.org/10.1182/blood.v126.23.3297.3297.

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Abstract BACKGROUND: While hematologic cancers comprise only 10% of all malignancies, they are divided into >100 distinct World Health Organization subtypes. It is known that higher volume of care is generally associated with better clinical outcomes. However, such a volume-outcome relationship in the medical management of hematologic cancers has not been rigorously explored. The American Society of Clinical Oncology (ASCO) National Census of Oncology Practices shows that the majority of hematologist-oncologists in the United States (US) have a combined hematology-oncology practice (J Oncol

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47

The, Enos, M. Jen Wajo, and M. A. Muin. "Respon fisiologis dan hematologis Kambing peranakan Etawah terhadap cekaman panas." Cassowary 1, no. 1 (2018): 63–74. http://dx.doi.org/10.30862/casssowary.cs.v1.i1.6.

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PE goat is a small ruminant crossed between Etawah goat and bean goat, which introduced in Manokwari since 2007. Livestock can well produce depend on environment comfortable temperature in the area of tropical temperature on the day is radiated in high sun light. If the goat is expose to the blazing sun, it supposed experiencing heat stress and caused to the physiological and haematological condition. The aim of this study is to know the physiological and haematological response of PE goat to heat stress. This design of research used is Split Plot (RPT). 8 goats will be a sample which devide i

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48

Kaiko, R., C. Cronin, and P. Goldenheim. "Hematologie safety associated with the administration of choline magnesium trisalcylate." European Journal of Pharmacology 183, no. 6 (1990): 2269–70. http://dx.doi.org/10.1016/0014-2999(90)93814-7.

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49

Tenner, Laura L., and Paul R. Helft. "Ethics in Oncology: An Annotated Bibliography of Important Literature." Journal of Oncology Practice 9, no. 4 (2013): e145-e153. http://dx.doi.org/10.1200/jop.2012.000679.

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50

Wagner, John E. "Practical and Ethical Issues with Genetic Screening." Hematology 2005, no. 1 (2005): 498–502. http://dx.doi.org/10.1182/asheducation-2005.1.498.

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Abstract Clinical hematologists are faced with a growing list of new genetic-based tools for identifying a patient’s risk of disease. While many of the disease-specific tests are readily available, validation studies are required. Furthermore, genetic-based tests are being pushed to their technical limits, such as testing a single cell prior to embryo selection and transfer for couples at risk of genetic disease. As a result, misdiagnosis or misinterpretation of the data may result. As new genetic testing opportunities proliferate, the hematologist needs to be aware of the medical and legal is

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