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Articles 56611 - 56640 of 62656
Full-Text Articles in Medicine and Health Sciences
The Immunology Of Transplantation, J. R. Serie
The Immunology Of Transplantation, J. R. Serie
Journal of the Minnesota Academy of Science
A number of life-threatening diseases, such as kidney failure, diabetes, and certain kinds of coronary heart disease, can be cured by organ transplantation. However, despite decades of research, graft rejection remains a very real threat to the organ transplant recipient. In attempting to develop methods that interfere with the graft rejection process, scientists have uncovered a remarkably complex system of cellular interactions that allows the total destruction of a transplanted organ while leaving the recipient's own organs untouched. This ability to distinguish self from non-self is achieved through intercellular communication involving cell-to-cell contact and the release of a number of …
Right To Know Legislation In Minnesota, Leo Uzych
Right To Know Legislation In Minnesota, Leo Uzych
Journal of the Minnesota Academy of Science
In June 1983, Minnesota approved a right to know law pertaining to the disclosure of information to workers about chemical hazards emanating from the workplace. A federal hazard communication disseminated in November 1983 may affect Minnesota's right to know law.
เภสัชวิทยาคลินิก (Clinical Pharmacology), มณฑิรา ตัณฑ์เกยูร
เภสัชวิทยาคลินิก (Clinical Pharmacology), มณฑิรา ตัณฑ์เกยูร
Chulalongkorn Medical Journal
No abstract provided.
Opiate Receptors และ Opioid Peptides, สำรวล สุทธิสีสังข์
Opiate Receptors และ Opioid Peptides, สำรวล สุทธิสีสังข์
Chulalongkorn Medical Journal
No abstract provided.
การใช้ Pulmonary Artery Catheter, วรรณา สมบูรณ์วิบูลย์
การใช้ Pulmonary Artery Catheter, วรรณา สมบูรณ์วิบูลย์
Chulalongkorn Medical Journal
No abstract provided.
การศึกษาผลการใช้ยา Cefadroxil ในโรคติดเชื้อแบคทีเรียของผิวหนัง, บุญนำ ลิ้มมงคล, นภดล นพคุณ
การศึกษาผลการใช้ยา Cefadroxil ในโรคติดเชื้อแบคทีเรียของผิวหนัง, บุญนำ ลิ้มมงคล, นภดล นพคุณ
Chulalongkorn Medical Journal
No abstract provided.
Anterolateral Harrington Instrumentation, Pibul Itiravivong
Anterolateral Harrington Instrumentation, Pibul Itiravivong
Chulalongkorn Medical Journal
No abstract provided.
ซิฟิลิสในระยะติดต่อ, พรทิพย์ หุยประเสริฐ, วิวัฒน์ ก่อกิจ, ธานี ศิริยง, S. Israsena
ซิฟิลิสในระยะติดต่อ, พรทิพย์ หุยประเสริฐ, วิวัฒน์ ก่อกิจ, ธานี ศิริยง, S. Israsena
Chulalongkorn Medical Journal
No abstract provided.
การศึกษาเอกสารเกี่ยวกับการพัฒนาชนบทด้านสุขภาพอนามัยของประเทศไทยระหว่างปี พ.ศ. 2514-2524, จันทนี อิทธิพานิชพงศ์, มณฑิรา ตัณฑ์เกยูร
การศึกษาเอกสารเกี่ยวกับการพัฒนาชนบทด้านสุขภาพอนามัยของประเทศไทยระหว่างปี พ.ศ. 2514-2524, จันทนี อิทธิพานิชพงศ์, มณฑิรา ตัณฑ์เกยูร
Chulalongkorn Medical Journal
No abstract provided.
J Am Coll Dent 1985 52 1
Journal of the American College of Dentists
The Journal of the American College of Dentists (JACD) publishes scholarly articles, editorials, essays, and reflections addressing the ethical, professional, and social dimensions of dentistry. The Journal serves as a forum for advancing ethics, professionalism, leadership, and excellence within the dental community. By fostering dialogue across disciplines and perspectives, JACD provides readers with insights that encourage ethical, professional practice, lifelong learning, and service to the public, reinforcing dentistry’s commitment to advancing oral healthcare and the common good.
Methemoglobin Reduction In The Presence Of Various Concentrations Of Oxyhemoglobin, Ali Mansouri
Methemoglobin Reduction In The Presence Of Various Concentrations Of Oxyhemoglobin, Ali Mansouri
Journal of the Arkansas Academy of Science
Methemoglobin reduction in human red blood cell is governed by many factors, one of which is the concentration of oxyhemoglobin. Experiments were conducted to determine the inhibition of methemoglobin reduction by oxyhemoglobin under concentrations approaching those in the red cell. Hemoglobin, methemoglobin reductase and cytochrome b₅ were prepared by routine protein purification methods. Methemoglobin reduction was carried out at 37° C in spectrophotometer. It is shown that methemoglobin concentration variation (at least when it is above 1 mM) does not change the reduction rate. Whereas, the ratio of methemoglobin to oxyhemoglobin determines the rate of methemoglobin reduction when all other …
Virginia Dental Journal (Vol. 62, No. 1, 1985)
Virginia Dental Journal (Vol. 62, No. 1, 1985)
Virginia Dental Journal
No abstract provided.
J Am Coll Dent 1985 52 2
Journal of the American College of Dentists
The Journal of the American College of Dentists (JACD) publishes scholarly articles, editorials, essays, and reflections addressing the ethical, professional, and social dimensions of dentistry. The Journal serves as a forum for advancing ethics, professionalism, leadership, and excellence within the dental community. By fostering dialogue across disciplines and perspectives, JACD provides readers with insights that encourage ethical, professional practice, lifelong learning, and service to the public, reinforcing dentistry’s commitment to advancing oral healthcare and the common good.
J Am Coll Dent 1985 52 4
Journal of the American College of Dentists
The Journal of the American College of Dentists (JACD) publishes scholarly articles, editorials, essays, and reflections addressing the ethical, professional, and social dimensions of dentistry. The Journal serves as a forum for advancing ethics, professionalism, leadership, and excellence within the dental community. By fostering dialogue across disciplines and perspectives, JACD provides readers with insights that encourage ethical, professional practice, lifelong learning, and service to the public, reinforcing dentistry’s commitment to advancing oral healthcare and the common good.
Linkage Data Excluding A Locus For Multiple Endocrine Neoplasia Type 2 Syndromes From The Distal Part Of The Short Arm Of Chromosome 11, Kenneth K. Kidd, Susan D. Kruger, Daniela S. Gerhard, Judith R. Kidd, David Housman, Joseph M. Gertner
Linkage Data Excluding A Locus For Multiple Endocrine Neoplasia Type 2 Syndromes From The Distal Part Of The Short Arm Of Chromosome 11, Kenneth K. Kidd, Susan D. Kruger, Daniela S. Gerhard, Judith R. Kidd, David Housman, Joseph M. Gertner
Henry Ford Hospital Medical Journal
A study designed to identify the location of a gene for multiple endocrine neoplasia type 2 (MEN-2) is being performed using a single large family segregating for MEN-2A. Here we report our initial results using a set of DNA restriction fragment length polymorphisms spanning a 40 cM segment of the short arm of human chromosome 11. The locus for MEN-2 in this family is excluded from this entire region which includes an oncogene, c-Ha-ras-1, two hormone loci, insulin and parathyroid, and the five hemoglobin genes in the beta hemoglobin gene duster. This is the first exclusion of such a large …
The First International Workshop On Multiple Endocrine Neoplasia Type 2 Syndromes, Charles E. Jackson
The First International Workshop On Multiple Endocrine Neoplasia Type 2 Syndromes, Charles E. Jackson
Henry Ford Hospital Medical Journal
No abstract provided.
Impact Of Screening On Prognosis In The Multiple Endocrine Neoplasia Type 2 Syndromes: Natural History And Treatment Results In 105 Patients, Margareta Telenius-Berg, Bertel Berg, Bertil Hamberger, Sten Tibblin, Lars-Erik Tisell, Lars Ysander, Gunnar Welander
Impact Of Screening On Prognosis In The Multiple Endocrine Neoplasia Type 2 Syndromes: Natural History And Treatment Results In 105 Patients, Margareta Telenius-Berg, Bertel Berg, Bertil Hamberger, Sten Tibblin, Lars-Erik Tisell, Lars Ysander, Gunnar Welander
Henry Ford Hospital Medical Journal
We evaluated the effects of screening for multiple endocrine neoplasia type 2A (MEN-2A) in 12 families. Genealogical studies going back to 1730 show a common ancestry for seven Swedish families and one American family. The total number of patients included 105 individuals, 68 of whom were diagnosed by our screening program. Our screening methods for medullary carcinoma of the thyroid (MTC) had an optimal sensitivity and specificity. The frequency of gene carriers detected in MEN-2A families was 55%. Screening will lead to early diagnosis and early therapy, which in turn, will significantly decrease morbidity, incidence of surgical complications, and mortality …
Central Registration Of Multiple Endocrine Neoplasia Type 2 Families In The Netherlands, C. J. M. Lips, E. Den Aantrekker, J. M. Jansen-Schillhorn Van Veen, R. A. Geerdink, G. Griffioen, E. A. Van Slooten
Central Registration Of Multiple Endocrine Neoplasia Type 2 Families In The Netherlands, C. J. M. Lips, E. Den Aantrekker, J. M. Jansen-Schillhorn Van Veen, R. A. Geerdink, G. Griffioen, E. A. Van Slooten
Henry Ford Hospital Medical Journal
No abstract provided.
Chromosomes In Multiple Endocrine Neoplasia Type 2 Syndromes, Daniel L. Van Dyke, V. Ramesh Babu, Charles E. Jackson
Chromosomes In Multiple Endocrine Neoplasia Type 2 Syndromes, Daniel L. Van Dyke, V. Ramesh Babu, Charles E. Jackson
Henry Ford Hospital Medical Journal
In 19 patients from nine MEN-2A families, high-resolution C-banded chromosome studies have revealed a visible deletion within sub-band 20p12.2, yet no abnormality was observed in a 10th family. A deletion indistinguishable from that in MEN-2A was observed in five patients from three MEN-2B families but not in two other MEN-2B families. We found no abnormality in the entire karyotype of the four MEN-1 patients studied. These findings suggest that the mutation in most MEN-2 patients is a visible deletion in the short arm of chromosome 20.
Research Vistas In The Multiple Endocrine Neoplasia Syndromes, John J. Mulvihill
Research Vistas In The Multiple Endocrine Neoplasia Syndromes, John J. Mulvihill
Henry Ford Hospital Medical Journal
Progress in understanding the single gene, cytogenetic, and multifactorial traits that predispose to human cancer suggests possible new directions for research in the multiple endocrine neoplasia (MEN) syndromes. Among the other 200 or so monogenic disorders associated with human neoplasia, advances have come from further delineation of syndromes by various clinical specialists, the recognition of subtypes of syndromes previously thought to be homogeneous, the search for in vitro manifestations of the mutant gene in fibroblasts, and the establishment of cell, tissue and patient registries and of voluntary lay organizations to serve as advocates for the disease. With regard to cytogenetics, …
Book Review: Medical Meanings, Fred W. Whitehouse
Book Review: Medical Meanings, Fred W. Whitehouse
Henry Ford Hospital Medical Journal
No abstract provided.
正常人與慢性神經根病變患者多相波之定量比較, 瑞棋 詹
正常人與慢性神經根病變患者多相波之定量比較, 瑞棋 詹
Rehabilitation Practice and Science
以電腦定量判讀方法檢查正常對象及慢性神經根病變患者,分別就肱三頭肌(biceps brachii)、總伸指肌(extenser digitorum communis)及脛前肌(anterior tibial-is)所出現之多相波,比較兩組對象之波幅(amplitude)、間期(duration)、多相波發生率、表面積(surface area)、相數(phases)、轉折數(Turns)及尖端期間(Peak-duration)、皆有明顯的統計學差異。本文並討論造成此差異之原因。
Severe Mental Retardation In Taiwan, R.O.C, I-Jen Loo
Severe Mental Retardation In Taiwan, R.O.C, I-Jen Loo
Rehabilitation Practice and Science
No abstract provided.
Multiple Endocrine Neoplasia Type 2 Syndromes: Historical Perspectives, John H. Sipple
Multiple Endocrine Neoplasia Type 2 Syndromes: Historical Perspectives, John H. Sipple
Henry Ford Hospital Medical Journal
No abstract provided.
The Calcitonin Assay And Multiple Endocrine Neoplasia Type 2 Syndromes: Historical Footnote, Kenneth E. W. Melvin
The Calcitonin Assay And Multiple Endocrine Neoplasia Type 2 Syndromes: Historical Footnote, Kenneth E. W. Melvin
Henry Ford Hospital Medical Journal
No abstract provided.
Register Of Multiple Endocrine Neoplasia Type 2 Syndromes In The United Kingdom, Bruce A. J. Ponder
Register Of Multiple Endocrine Neoplasia Type 2 Syndromes In The United Kingdom, Bruce A. J. Ponder
Henry Ford Hospital Medical Journal
A collaborative group for the study of multiple endocrine neoplasia type 2 (MEN-2) syndromes comprised of clinicians and laboratory scientists has been set up in the United Kingdom. Its aims are 1) to provide a basis for collaborative work on MEN-2; 2) to establish a register of patients; 3) and specifically to conduct studies aimed at defining the best policy for screening the families of apparently sporadic patients, to establish radioimmunoassays for family screening, and to identify large kindreds for genetic linkage studies using DNA polymorphisms.
Screening For Hereditary Medullary Cancer In Denmark, Kristian Emmertsen
Screening For Hereditary Medullary Cancer In Denmark, Kristian Emmertsen
Henry Ford Hospital Medical Journal
Screening of first-degree relatives of patients with medullary thyroid cancer (MTC) gave normal values of pentagastrin-stimulated serum calcitonin and 24-hour urinary catecholamine levels in the relatives of 18 of 22 patients. This result is considered to be valid evidence for sporadic MTC. Absence of C-cell hyperplasia maybe another indication of sporadic MTC. Four hereditary MTCs were represented by one fully expressed MEN-2B patient without affected relatives, one fully expressed MEN-2A case in one family, and two first cousins with MTC as the only MEN-2A lesion in another family. Fourteen relatives of the MEN-2A patients had elevated serum calcitonin levels, and …
Familial Medullary Carcinoma Of The Thyroid: Clinical Studies In Northern New England, Walter W. Noll, L. Herbert Maurer, Victoria L. Herzberg, Paul J. Beisswenger, Brian M. Quinn, Charles C. Cate, Jane P. Bassick, Patricia A. Clark, Thomas A. Colacchio
Familial Medullary Carcinoma Of The Thyroid: Clinical Studies In Northern New England, Walter W. Noll, L. Herbert Maurer, Victoria L. Herzberg, Paul J. Beisswenger, Brian M. Quinn, Charles C. Cate, Jane P. Bassick, Patricia A. Clark, Thomas A. Colacchio
Henry Ford Hospital Medical Journal
No abstract provided.
Multiple Endocrine Neoplasia Type 2 Syndromes In Japan, Shin-Ichiro Takai, Akira Miyauchi, Hideo Matsumoto, Tatsuro Ikeuchi, Tetsuro Miki, Kanji Kuma, Yuichi Kumahara
Multiple Endocrine Neoplasia Type 2 Syndromes In Japan, Shin-Ichiro Takai, Akira Miyauchi, Hideo Matsumoto, Tatsuro Ikeuchi, Tetsuro Miki, Kanji Kuma, Yuichi Kumahara
Henry Ford Hospital Medical Journal
Through nationwide surveys, we collected and analyzed 242 patients of medullary thyroid carcinoma (MTC). Included were 40 patients with multiple endocrine neoplasia type 2A (MEN-2A), six patients with MEN-2B, and 36 patients with only MTC having a positive family history (82 total patients in the hereditary group). Ten-year survival rates were 81.5% for all cases, and 97.5% and 76.1% for the hereditary and the sporadic group, respectively. Epinephrine/norepinephrine ratio in the urine was found to be a good indicator of the adrenomedullary hyperfunction in patients with hereditary MTC. At least one patient in each family with hereditary MTC had overt …