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• I. Axial Images of Cadaver and Human Brain of 7.0T MRI in vivo II. Sagittal Images of Cadaver and Human Brain of 7.0T MRI in vivo III. Coronal Images of Cadaver and Human Brain of 7.0T MRI in vivo.
• (source: Nielsen Book Data)

Recent advances in MRI, especially those in the area of ultra high field (UHF) MRI, have attracted significant attention in the field of brain imaging for neuroscience research, as well as for clinical applications. In "7.0 Tesla MRI Brain Atlas: In Vivo Atlas with Cryomacrotome Correlation", Zang Hee Cho and his colleagues at the Neuroscience Research Institute, Gachon University of Medicine and Science set new standards in neuro-anatomy. This unprecedented atlas presents the future of MR imaging of the brain. Taken at 7.0 Tesla, the images are of a live subject with correlating cryomacrotome photographs. Exquisitely produced in an oversized format to allow careful examination of the brain in real scale, each image is precisely annotated and detailed. The images in the Atlas reveal a wealth of details of the main stem and midbrain structures that were once thought impossible to visualize in-vivo. Ground breaking and thought provoking, "7.0 Tesla MRI Brain Atlas" is sure to provide answers and inspiration for further studies, and is a valuable resource for medical libraries, neuroradiologists and neuroscientists.
(source: Nielsen Book Data)

• I.- Skull.- Thorax.- Spine.- Pelvis.- Long Bones.- Hands.- Feet.- Joints.- Generalized Skeletal Abnormalities.- II.- Aarskog Syndrome.- Achondrogenesis, Type IB.- Achondrogenesis, Type II.- Achondroplasia.- Acrofacial Dysostosis, Nager Type.- Angelman Syndrome.- Apert Syndrome.- Asphyxiating Thoracic Dysplasia.- Atelosteogenesis.- Bardet-Biedl Syndrome.- Beckwith-Wiedemann Syndrome.- C Syndrome.- Campomelic Dysplasia.- Carpenter Syndrome.- Cerebro-costo-mandibular Syndrome.- CHARGE Association.- Chondrodysplasia Punctata, Conradi-Hunermann Type.- Chondrodysplasia Punctata, Rhizomelic Type.- Chondrodysplasia Punctata, Brachytelephalangic Type.- Chondroectodermal Dysplasia.- Chromosome 4p- Syndrome.- Chromosome Trisomy 13 Syndrome.- Chromosome Trisomy 18 Syndrome.- Chromosome Trisomy 21 Syndrome.- Cleidocranial Dysplasia.- Cockayne Syndrome.- Coffin-Lowry Syndrome.- Coffin-Siris Syndrome.- Cohen Syndrome.- Craniometaphyseal Dysplasia, Dominant Type.- Cri-du-chat Syndrome.- Crouzon Syndrome.- De Lange Syndrome.- Diaphyseal Dysplasia.- Diastrophic Dysplasia.- Dubowitz Syndrome.- Dyschondrosteosis.- Dysosteosclerosis.- Ectodermal Dysplasias.- Ehlers-Danlos Syndromes.- Enchondromatosis.- Exostoses, Multiple.- Fanconi Anemia.- Focal Dermal Hypoplasia Syndrome.- Freeman-Sheldon Syndrome.- Frontometaphyseal Dysplasia.- Goldenhar Syndrome.- Hallermann-Streiff Syndrome.- Holt-Oram Syndrome.- Kenny-Caffey Syndrome.- Klippel-Feil Anomaly.- Klippel-Trenaunay-Weber Syndrome.- Kniest Dysplasia.- Larsen Syndrome.- Marfan Syndrome.- McCune-Albright Syndrome.- Meckel Syndrome.- Melnick-Needles Syndrome.- Melorheostosis.- Mental Retardation, X-Linked, Associated with FRA Xq27.3.- Mesomelic Dwarfism, Langer Type.- Mesomelic Dwarfism, Nievergelt Type.- Metatropic Dysplasia.- Multiple Epiphyseal Dysplasia.- Nail-Patella Syndrome.- Nevoid Basal Cell Carcinoma Syndrome.- Noonan Syndrome.- Opitz Syndrome.- Oro-facio-digital Syndrome, Type I.- Oro-facio-digital Syndrome, Type II.- Osteogenesis Imperfecta, Type I.- Osteogenesis Imperfecta, Type IIA.- Osteogenesis Imperfecta, Type IIB/III.- Osteopathia Striata with Cranial Sclerosis.- Osteopetrosis, Infantile Type.- Osteopetrosis, Adult Type.- Osteopoikilosis.- Oto-palato-digital Syndrome, Type I.- Oto-palato-digital Syndrome, Type II.- Pena-Shokeir Syndrome.- Pfeiffer Syndrome.- Poland Syndrome.- Prader-Willi Syndrome.- Progeria.- Pseudoachondroplasia.- Pyknodysostosis.- Roberts Syndrome.- Robin Sequence.- Robinow Syndrome.- Rubinstein-Taybi Syndrome.- Saethre-Chotzen Syndrome.- Seckel Syndrome.- Short Rib-Polydactyly Syndrome, Type I.- Short Rib-Polydactyly Syndrome, Type II.- Silver-Russell Syndrome.- Smith-Lemli-Opitz Syndrome.- Sotos Syndrome.- Spondyloepimetaphyseal Dysplasia, Irapa Type.- Spondyloepimetaphyseal Dysplasia, Strudwick Type.- Spondyloepiphyseal Dysplasia Congenita.- Spondyloepiphyseal Dysplasia Tarda.- Spondylometaphyseal Dysplasia, Kozlowski Type.- Stickler Syndrome.- Thanatophoric Dysplasia.- Thrombocytopenia-Absent Radius Syndrome.- Treacher-Collins Syndrome.- Tricho-rhino-phalangeal Syndrome, Type I.- Tricho-rhino-phalangeal Syndrome, Type II.- Turner Syndrome.- VATER Association.- Williams Syndrome.
• (source: Nielsen Book Data)

Taking a symptom-oriented approach, this book focuses on the radiographic changes of malformation syndromes and skeletal dysplasias. Its clear structure makes it an essential, practical guide for radiologists, geneticists, and pediatricians.
(source: Nielsen Book Data)

Through a narrative consisting of ministories, quotes, interviews of anthropological and sociological experts, and stunning graphics, this book traces the evolution of our faces and our incredible ability to recognize and read other individuals no matter how they disguise themselves by glasses, makeup, and the like. 117 photos and line art. Published to coincide with a major exhibit touring America.
(source: Nielsen Book Data)

The first article is Cowper's description of the glands which bear his name. He was forestalled in their discovery by Jean Méry.

• Trunk : body wall and spine
• Thorax
• Abdomen
• Pelvis and perineum
• Lower limb
• Upper limb
• Head and neck
• Cranial and autonomic nerves.

This second edition features full-color art throughout, using a three-dimensional approach to anatomic structure. Emphasizing surface anatomy, it features unique additional views (posterior, medial, lateral) of important structures with extensive coverage of those areas--such as the perineum, head, and neck--which are often difficult for students to understand and appreciate.