標(biāo)題: Titlebook: Diagnostic Molecular Pathology in Practice; A Case-Based Approac Iris Schrijver Book 2011 Springer-Verlag Berlin Heidelberg 2011 Hematopath [打印本頁] 作者: BULB 時(shí)間: 2025-3-21 18:48
書目名稱Diagnostic Molecular Pathology in Practice影響因子(影響力)
書目名稱Diagnostic Molecular Pathology in Practice影響因子(影響力)學(xué)科排名
書目名稱Diagnostic Molecular Pathology in Practice網(wǎng)絡(luò)公開度
書目名稱Diagnostic Molecular Pathology in Practice網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Diagnostic Molecular Pathology in Practice被引頻次
書目名稱Diagnostic Molecular Pathology in Practice被引頻次學(xué)科排名
書目名稱Diagnostic Molecular Pathology in Practice年度引用
書目名稱Diagnostic Molecular Pathology in Practice年度引用學(xué)科排名
書目名稱Diagnostic Molecular Pathology in Practice讀者反饋
書目名稱Diagnostic Molecular Pathology in Practice讀者反饋學(xué)科排名
作者: Diastole 時(shí)間: 2025-3-21 22:17
Polycystic Kidney DiseaseADPKD, her mother underwent unilateral nephrectomy during childhood for an unknown indication. The patient had three siblings; both sisters had negative screening renal ultrasonography after age 40 and her 36-year-old brother had not been evaluated. There was a three pack-year history of tobacco use作者: parsimony 時(shí)間: 2025-3-22 00:40 作者: interrogate 時(shí)間: 2025-3-22 05:49
B-Cell Lymphomaa antigen), CD20 (mature B-cell marker), CD21 (part of the B-cell coreceptor complex, positive on follicular dendritic cells), CD30 (marker of activated B and T cells), CD45 (leukocyte common antigen), CD57 (human natural killer-1 protein), and BCL2 (B-cell lymphoma-2 protein, antiapoptotic protein)作者: 火車車輪 時(shí)間: 2025-3-22 10:37
Acute Myeloid Leukemia: ,/, and thrombocytopenia. Upon review of the peripheral smear, the pathologist noted moderate anisopoikilocytosis of the red cells and rare circulating blasts. On aspirate smear, an increase in blasts was identified comprising approximately 30% of total nucleated cells. Erythroid precursors were markedl作者: Gum-Disease 時(shí)間: 2025-3-22 16:49
Book 2011minations. It will also be very useful for residents and fellows in medical specialties to which MGP is pertinent, and for practicing pathologists who want to learn more about the current practice of molecular diagnostics..作者: Gum-Disease 時(shí)間: 2025-3-22 17:35 作者: Ergots 時(shí)間: 2025-3-23 01:18
Carsten Rennhak,Marion Halfmann 23%, elevated reticulocytes, hyperbilirubinemia and an RhD-positive phenotype with a 3+ direct anti-globulin test (DAT) result. The DAT result, also known as the direct Coombs test, indicated that the fetal red cells were coated with maternal alloantibodies. The fetus was treated with intrauterine 作者: 厭食癥 時(shí)間: 2025-3-23 01:23
Darstellung der Forschungsfragen,a antigen), CD20 (mature B-cell marker), CD21 (part of the B-cell coreceptor complex, positive on follicular dendritic cells), CD30 (marker of activated B and T cells), CD45 (leukocyte common antigen), CD57 (human natural killer-1 protein), and BCL2 (B-cell lymphoma-2 protein, antiapoptotic protein)作者: ELUDE 時(shí)間: 2025-3-23 09:31 作者: MENT 時(shí)間: 2025-3-23 09:54
,Das Organisationskonzept für ein Intranet,was deaf. They were also contemplating another pregnancy and sought to learn about the risk of having a second child with hearing loss. The patient’s mother had northern European ancestry, whereas the father was of Ashkenazi Jewish extraction.作者: Graphite 時(shí)間: 2025-3-23 14:36
Amparo Gali?anes Garcia,Carsten Rennhakitial prenatal visit she discussed fragile X testing with her physician, having read about it in a popular magazine. Although Linda’s first child did not have fragile X syndrome and there was no history of mental retardation or autism-spectrum disorders in her family, she requested carrier screening for fragile X syndrome.作者: 獸皮 時(shí)間: 2025-3-23 20:05 作者: Nonporous 時(shí)間: 2025-3-24 01:06
Andreas Günther,Martina Hasselerection and over the ensuing seven years had not been regularly compliant with his highly active antiretroviral therapy (HAART). Past medical history was significant for hypertension, type 2 diabetes mellitus, and a poorly defined seizure disorder.作者: watertight, 時(shí)間: 2025-3-24 05:27
https://doi.org/10.1007/978-3-642-19677-5Hematopathology; Infectious Disease; Oncology作者: bioavailability 時(shí)間: 2025-3-24 07:54
978-3-642-19676-8Springer-Verlag Berlin Heidelberg 2011作者: 彩色 時(shí)間: 2025-3-24 14:44
Hearing Losswas deaf. They were also contemplating another pregnancy and sought to learn about the risk of having a second child with hearing loss. The patient’s mother had northern European ancestry, whereas the father was of Ashkenazi Jewish extraction.作者: COKE 時(shí)間: 2025-3-24 16:06
Fragile X Syndromeitial prenatal visit she discussed fragile X testing with her physician, having read about it in a popular magazine. Although Linda’s first child did not have fragile X syndrome and there was no history of mental retardation or autism-spectrum disorders in her family, she requested carrier screening for fragile X syndrome.作者: FACT 時(shí)間: 2025-3-24 19:55
T-Cell Lymphoma chronic dermatitis. Physical exam revealed that approximately 10% of her body surface was involved by red to brown scaly patches. No lymphadenopathy or hepatosplenomegaly was present. A biopsy of the involved skin was obtained. Complete blood count and peripheral blood flow cytometry were within normal limits.作者: 平庸的人或物 時(shí)間: 2025-3-24 23:17
HIV-Associated Hodgkin Lymphomaection and over the ensuing seven years had not been regularly compliant with his highly active antiretroviral therapy (HAART). Past medical history was significant for hypertension, type 2 diabetes mellitus, and a poorly defined seizure disorder.作者: crumble 時(shí)間: 2025-3-25 04:18 作者: CARE 時(shí)間: 2025-3-25 11:03 作者: 讓空氣進(jìn)入 時(shí)間: 2025-3-25 13:35 作者: sleep-spindles 時(shí)間: 2025-3-25 16:04 作者: 變形 時(shí)間: 2025-3-25 20:35 作者: 貞潔 時(shí)間: 2025-3-26 02:09
Generationenfrage Kundenloyalit?t?D at age 36 after developing fever and flank pain. At that time, ultrasonography showed bilateral renal cysts, and liver and ovarian cysts. The serum creatinine level was normal. Hypertension was diagnosed at the age of 32 years and has since been controlled by treatment with an angiotensin converti作者: Microaneurysm 時(shí)間: 2025-3-26 07:59 作者: 得罪人 時(shí)間: 2025-3-26 10:21 作者: 最低點(diǎn) 時(shí)間: 2025-3-26 16:21
Carsten Rennhak,Marion Halfmannbody screen was negative at 15 weeks and remained negative during repeat screens at monthly intervals. The patient was treated with Rh immune globulin (RhIG) at 28 weeks. She went into labor at 40 weeks. The infant was RhD-positive and RhIG was administered to the mother. One year later, the patient作者: 預(yù)兆好 時(shí)間: 2025-3-26 17:22 作者: Hallmark 時(shí)間: 2025-3-26 22:46 作者: 驚呼 時(shí)間: 2025-3-27 01:52 作者: negligence 時(shí)間: 2025-3-27 07:22
Agnes Neumayr,Michael Baubin,Adolf Schinnerlcated that the patient is homozygous for the c.1521.1523delCTT [p.Phe508del] mutation. One brother died of cystic fibrosis at the age of two years. Since the time of transplantation, the patient has been on immunosuppressive therapy (azathioprine and cyclosporine) to prevent graft rejection. Then th作者: 放縱 時(shí)間: 2025-3-27 11:36
Andreas Günther,Martina Hasselerection and over the ensuing seven years had not been regularly compliant with his highly active antiretroviral therapy (HAART). Past medical history was significant for hypertension, type 2 diabetes mellitus, and a poorly defined seizure disorder.作者: Nucleate 時(shí)間: 2025-3-27 15:46 作者: 扔掉掐死你 時(shí)間: 2025-3-27 21:34
Wolfgang Lück,Michael Henke,Philipp Gaenslenn by her primary care physician with complaints of intermittent mild night sweats, frequent vasomotor symptoms such as hot flashes, and early satiety with abdominal fullness and pain if she laid on her right side. Laboratory evaluation at that time revealed a hematocrit of 57.6% (reference interval 作者: 昏睡中 時(shí)間: 2025-3-27 22:20 作者: 重畫只能放棄 時(shí)間: 2025-3-28 05:07
Iris SchrijverPractical, case-based format.Covers a wide range of issues frequently encountered by the molecular genetic pathologist.Ideal aid to practice-based preparation for board examinations.Includes supplemen作者: Narcissist 時(shí)間: 2025-3-28 08:38 作者: surmount 時(shí)間: 2025-3-28 11:48 作者: 孤獨(dú)無助 時(shí)間: 2025-3-28 15:17
Wolfgang Lück,Michael Henke,Philipp Gaenslen/?L). She was treated with phlebotomy alone for approximately two years. However, she continued to have persistent erythrocytosis and during her last checkup was found to have an elevated platelet count of 915,000/?L (reference interval 150,000–450,000/?L).作者: Cytology 時(shí)間: 2025-3-28 21:22
Charcot-Marie-Tooth Disease hydrocephalus with excess subdural fluid and increased ventricular size. An electro-encephalogram (EEG) was normal, as was a laboratory workup which included creatine phosphokinase, lactate, and pyruvate levels as well as urine organic acids.作者: sleep-spindles 時(shí)間: 2025-3-29 02:53
Myeloproliferative Neoplasms/?L). She was treated with phlebotomy alone for approximately two years. However, she continued to have persistent erythrocytosis and during her last checkup was found to have an elevated platelet count of 915,000/?L (reference interval 150,000–450,000/?L).作者: Mendacious 時(shí)間: 2025-3-29 03:23
Book 2011 genetic pathologist. The book is divided into four sections on the principal areas addressed in molecular genetic pathology (MGP): inherited diseases, hematopathology, solid tumors, and infectious diseases. The topics covered by the cases in each section include test selection, qualitative and quan作者: FATAL 時(shí)間: 2025-3-29 10:26 作者: 搖曳 時(shí)間: 2025-3-29 12:34 作者: 行為 時(shí)間: 2025-3-29 15:57 作者: Brain-Waves 時(shí)間: 2025-3-29 21:48 作者: 不真 時(shí)間: 2025-3-30 03:47
https://doi.org/10.1007/978-3-658-39551-3icant for a mildly elevated white blood cell count, creatine kinase of 541 U/L (normal 70–185 U/L), CK-MB of 78.4 ng/mL (normal <6.0 ng/mL), and troponin I of 4.53 ng/mL (normal <0.034 ng/mL), consistent with myocardial infarction.作者: 愚笨 時(shí)間: 2025-3-30 07:37
Cystic Fibrosisnegative family history. Although some physicians offer couples-based tested initially, a typical approach is maternal testing followed by assessment of need for paternal testing based on the maternal result. At 16 weeks gestation, prenatal ultrasound identified an echogenic bowel abnormality.作者: PAC 時(shí)間: 2025-3-30 11:15 作者: ALIAS 時(shí)間: 2025-3-30 12:28
Pharmacogeneticsicant for a mildly elevated white blood cell count, creatine kinase of 541 U/L (normal 70–185 U/L), CK-MB of 78.4 ng/mL (normal <6.0 ng/mL), and troponin I of 4.53 ng/mL (normal <0.034 ng/mL), consistent with myocardial infarction.作者: 網(wǎng)絡(luò)添麻煩 時(shí)間: 2025-3-30 18:42
Alpha ThalassemiaIron studies were normal, and the normal HbA. results effectively ruled out beta thalassemia trait. DNA testing for alpha thalassemia was therefore performed, but both parents were negative for six common deletional mutations that cause most cases of alpha thalassemia.作者: periodontitis 時(shí)間: 2025-3-31 00:23
Malignant Hyperthermiading bolus of 2.5 mg/kg intravenous dantrolene, an antidote to MH-triggering agents. Subsequent bolus doses of 1 mg/kg were administered intravenously until the signs of acute MH abated and the ETCO. normalized. The patient had an unconfirmed family history of a similar episode in a maternal uncle.作者: 消息靈通 時(shí)間: 2025-3-31 04:33
Chronic Myelogenous Leukemiaof presentation are shown in Table 15.1. The patient underwent a bone marrow biopsy which also showed increased granulocytic precursors with maturation (Fig. 15.1a). The patient’s family history was negative for any hematologic disorders.作者: 非實(shí)體 時(shí)間: 2025-3-31 05:02
Posttransplant Lymphoproliferative Disordernce the time of transplantation, the patient has been on immunosuppressive therapy (azathioprine and cyclosporine) to prevent graft rejection. Then the patient presented with a fever unresponsive to anti-biotics. Physical examination revealed abdominal lym-phadenopathy.作者: 支柱 時(shí)間: 2025-3-31 11:54
Josef Ehmer,Ursula Ferdinand,Jürgen ReuleckeIron studies were normal, and the normal HbA. results effectively ruled out beta thalassemia trait. DNA testing for alpha thalassemia was therefore performed, but both parents were negative for six common deletional mutations that cause most cases of alpha thalassemia.作者: peritonitis 時(shí)間: 2025-3-31 14:58 作者: 討厭 時(shí)間: 2025-3-31 20:18
https://doi.org/10.1007/978-3-662-56627-5of presentation are shown in Table 15.1. The patient underwent a bone marrow biopsy which also showed increased granulocytic precursors with maturation (Fig. 15.1a). The patient’s family history was negative for any hematologic disorders.
