Häftad, Engelska
206 kr
Skickas inom 3-6 vardagar
K. Michael Gibson – författare
Visar alla böcker från författaren K. Michael Gibson. Handla med fri frakt och snabb leverans.
27 produkter
27 produkter
- Häftad, Engelska, 2015
269 kr
Skickas inom 3-6 vardagar
- Del 12 - JIMD Reports
JIMD Reports - Volume 12
Häftad, Engelska, 2014563 kr
Skickas inom 10-15 vardagar
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2014
732 kr
Läs direkt efter köp
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2008
1 902 kr
Läs direkt efter köp
- Del 7 - JIMD Reports
JIMD Reports - Case and Research Reports, 2012/4
Häftad, Engelska, 2012563 kr
Skickas inom 10-15 vardagar
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2012
732 kr
Läs direkt efter köp
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - Del 8 - JIMD Reports
JIMD Reports - Case and Research Reports, 2012/5
Häftad, Engelska, 20121 118 kr
Skickas inom 10-15 vardagar
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2012
1 459 kr
Läs direkt efter köp
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - Del 9 - JIMD Reports
JIMD Reports - Case and Research Reports, 2012/6
Häftad, Engelska, 20121 285 kr
Skickas inom 10-15 vardagar
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokEngelska, 2012
1 682 kr
Läs direkt efter köp
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - Del 11 - JIMD Reports
JIMD Reports - Volume 11
Häftad, Engelska, 20131 118 kr
Skickas inom 10-15 vardagar
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2013
1 455 kr
Läs direkt efter köp
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - Del 10 - JIMD Reports
JIMD Reports - Volume 10
Häftad, Engelska, 20131 118 kr
Skickas inom 10-15 vardagar
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2013
1 455 kr
Läs direkt efter köp
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2014
2 917 kr
Läs direkt efter köp
This book, combining and updating two previous editions, is a unique source of information on the diagnosis, treatment, and follow-up of metabolic diseases. The clinical and laboratory data characteristic of rare metabolic conditions can be bewildering for both clinicians and laboratory personnel. Reference laboratory data are scattered, and clinical descriptions may be obscure. The Physician’s Guide documents the features of more than five hundred conditions, grouped according to type of disorder, organ system affected (e.g. liver, kidney, etc) or phenotype (e.g. neurological, hepatic, etc). Relevant clinical findings are provided and pathological values for diagnostic metabolites highlighted. Guidance on appropriate biochemical genetic testing is provided. Established experimental therapeutic protocols are described, with recommendations on follow-up and monitoring. The authors are acknowledged experts, and the book will be a valuable desk reference for all who deal with inherited metabolic diseases.
- Del 13 - JIMD Reports
JIMD Reports - Case and Research Reports, Volume 13
Häftad, Engelska, 20141 118 kr
Skickas inom 10-15 vardagar
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2014
1 455 kr
Läs direkt efter köp
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - Del 14 - JIMD Reports
JIMD Reports, Volume 14
Häftad, Engelska, 20141 118 kr
Skickas inom 10-15 vardagar
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2014
1 455 kr
Läs direkt efter köp
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - Del 15 - JIMD Reports
JIMD Reports, Volume 15
Häftad, Engelska, 20151 118 kr
Skickas inom 10-15 vardagar
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2014
1 455 kr
Läs direkt efter köp
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - Del 17 - JIMD Reports
JIMD Reports, Volume 17
Häftad, Engelska, 2014563 kr
Skickas inom 10-15 vardagar
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2014
732 kr
Läs direkt efter köp
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - Del 16 - JIMD Reports
JIMD Reports Volume 16
Häftad, Engelska, 2014563 kr
Skickas inom 10-15 vardagar
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - E-bokPDF, Engelska, 2014
734 kr
Läs direkt efter köp
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder. - Häftad, Engelska, 2016
2 384 kr
Skickas inom 11-20 vardagar
This book, combining and updating two previous editions, is a unique source of information on the diagnosis, treatment, and follow-up of metabolic diseases. The clinical and laboratory data characteristic of rare metabolic conditions can be bewildering for both clinicians and laboratory personnel. Reference laboratory data are scattered, and clinical descriptions may be obscure. The Physician’s Guide documents the features of more than five hundred conditions, grouped according to type of disorder, organ system affected (e.g. liver, kidney, etc) or phenotype (e.g. neurological, hepatic, etc). Relevant clinical findings are provided and pathological values for diagnostic metabolites highlighted. Guidance on appropriate biochemical genetic testing is provided. Established experimental therapeutic protocols are described, with recommendations on follow-up and monitoring. The authors are acknowledged experts, and the book will be a valuable desk reference for all who deal with inherited metabolic diseases.
