K. Michael Gibson – författare
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26 produkter
26 produkter
Häftad, Engelska, 2015
263 kr
Skickas inom 3-6 vardagar
Del 12 - JIMD Reports
JIMD Reports - Volume 12
Häftad, Engelska, 2014
566 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-bok
PDF, Engelska, 2014708 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-bok
PDF, Engelska, 20081 840 kr
Läs direkt efter köp
Del 7 - JIMD Reports
JIMD Reports - Case and Research Reports, 2012/4
Häftad, Engelska, 2012
566 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-bok
PDF, Engelska, 2012714 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, 2012
1 124 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-bok
PDF, Engelska, 20121 408 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, 2012
1 292 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-bok
Engelska, 20121 628 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, 2013
1 124 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-bok
PDF, Engelska, 20131 408 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, 2013
1 124 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-bok
PDF, Engelska, 20131 408 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-bok
PDF, Engelska, 20142 822 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, 2014
1 124 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-bok
PDF, Engelska, 20141 420 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, 2014
1 124 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-bok
PDF, Engelska, 20141 408 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, 2015
1 124 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-bok
PDF, Engelska, 20141 408 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, 2014
566 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-bok
PDF, Engelska, 2014708 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, 2014
566 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-bok
PDF, Engelska, 2014708 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
2 241 kr
Skickas inom 10-15 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.