Diagnostic Imaging Pediatric Neuroradiology 3rd edition by Kevin Moore ISBN 0323708552 9780323708555

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ISBN 10:0323708552

ISBN 13:9780323708555

Author: Kevin Moore 

Covering the entire spectrum of this fast-changing field, Diagnostic Imaging: Pediatric Neuroradiology, third edition,is an invaluable resource for radiologists, child neurologists, and pediatricians―anyone who requires an easily accessible reference that covers common and uncommon disorders affecting the brain, head, neck, and spine of children. Dr. Kevin Moore and an expert author team provide carefully updated information and an abundance of high-quality images throughout, making this edition a useful learning tool as well as a handy reference source for daily practice.

• Features more than 2,300 annotated images, including MR, CT, proton spectroscopy, and angiographic findings
• Brings you up to speed with recent name changes and reclassification of both neoplastic and nonneoplastic central nervous system (CNS) entities, revised classification of tumor types/subtypes, changes in metabolic disorders and malformations, and entirely new disorders and groups of disorders such as acute flaccid myelitis
• Includes new chapters covering important pediatric spine neoplasms, such as CNS intradural tumor dissemination and myxopapillary ependymoma
• Provides expanded coverage of better-understood genetic white matter diseases such as vanishing white matter disease
• Discusses key topics such as newly discovered genetic mutations correlating with distinct imaging appearances and prognosis, newly characterized infectious entities, recent descriptions of important Chiari I malformation variants, newly described entities based on genetics in addition to histological features, and advances in the diagnosis of abusive head trauma
• Uses bulleted, succinct text for fast and easy comprehension of essential information, including terminology, imaging findings, key facts, differential diagnosis, pathology, clinical issues, diagnostic checklist, and selected references
• Includes an extensive image gallery for each entity, depicting common and variant cases
• Offers a vivid, full-color design that makes the material easy to read
• Displays a “thumbnail” visual differential diagnosis for each entity
• Enhanced eBook version included with purchase, which allows you to access all of the text, figures, and references from the book on a variety of devices

Diagnostic Imaging Pediatric Neuroradiology 3rd Table of Contents:

1. Part I: Brain
2. SECTION 1: PATHOLOGY-BASED DIAGNOSES
3. CONGENITAL MALFORMATIONS
4. Chapter 1: Approach to Brain Malformations
5. HINDBRAIN MALFORMATIONS
6. Chapter 2: Dandy-Walker Continuum
7. Chapter 3: Rhombencephalosynapsis
8. Chapter 4: Unclassified Cerebellar Dysplasias
9. Chapter 5: Molar Tooth Malformations (Joubert)
10. Chapter 6: Cerebellar Dysplastic Gangliocytoma
11. Chapter 7: Cerebellar Hypoplasia
12. DISORDERS OF DIVERTICULATION/CLEAVAGE
13. Chapter 8: Holoprosencephaly
14. Chapter 9: Syntelencephaly (Middle Interhemispheric Variant)
15. Chapter 10: Septo-Optic Dysplasia
16. Chapter 11: Commissural Abnormalities
17. MALFORMATIONS OF CORTICAL DEVELOPMENT
18. Chapter 12: Congenital Microcephaly
19. Chapter 13: Congenital Muscular Dystrophy
20. Chapter 14: Heterotopic Gray Matter
21. Chapter 15: Polymicrogyria
22. Chapter 16: Focal Cortical Dysplasia
23. Chapter 17: Lissencephaly
24. Chapter 18: Schizencephaly
25. Chapter 19: Hemimegalencephaly
26. Chapter 20: DNET
27. FAMILIAL TUMOR/NEUROCUTANEOUS SYNDROMES
28. Chapter 21: Neurofibromatosis Type 1, Brain
29. Chapter 22: Neurofibromatosis Type 2, Brain
30. Chapter 23: von Hippel-Lindau Syndrome
31. Chapter 24: Tuberous Sclerosis Complex
32. Chapter 25: Sturge-Weber Syndrome
33. Chapter 26: Meningioangiomatosis
34. Chapter 27: Basal Cell Nevus Syndrome
35. Chapter 28: Neurocutaneous Melanosis
36. Chapter 29: Hereditary Hemorrhagic Telangiectasia
37. Chapter 30: Encephalocraniocutaneous Lipomatosis
38. TRAUMA
39. Chapter 31: Neonatal Subpial Hemorrhage
40. Chapter 32: Epidural Hematoma, Classic
41. Chapter 33: Acute Subdural Hematoma
42. Chapter 34: Evolving Subdural Hematoma
43. Chapter 35: Cerebral Contusion
44. Chapter 36: Diffuse Axonal Injury
45. Chapter 37: Subcortical Injury
46. Chapter 38: Abusive Head Trauma
47. STROKE
48. Chapter 39: Germinal Matrix Hemorrhage
49. Chapter 40: Hydranencephaly
50. Chapter 41: White Matter Injury of Prematurity
51. Chapter 42: Hypoxic-Ischemic Encephalopathy
52. Chapter 43: Childhood Stroke
53. Chapter 44: Sickle Cell Disease, Brain
54. Chapter 45: Moyamoya
55. VASCULAR MALFORMATIONS: CVMS WITH AV SHUNTING
56. Chapter 46: Arteriovenous Malformation
57. Chapter 47: Dural Arteriovenous Fistula
58. Chapter 48: Vein of Galen Aneurysmal Malformation
59. CVMS WITHOUT AV SHUNTING
60. Chapter 49: Developmental Venous Anomaly
61. Chapter 50: Sinus Pericranii
62. Chapter 51: Cavernous Malformation
63. Chapter 52: Capillary Telangiectasia
64. NEOPLASMS: ASTROCYTIC TUMORS
65. Chapter 53: Pilocytic Astrocytoma
66. Chapter 54: Pilomyxoid Astrocytoma
67. Chapter 55: Anaplastic Astrocytoma
68. Chapter 56: Glioblastoma
69. Chapter 57: Subependymal Giant Cell Astrocytoma
70. Chapter 58: Brainstem Tumors
71. Chapter 59: Diffuse Intrinsic Pontine Glioma
72. Chapter 60: Pleomorphic Xanthoastrocytoma
73. EPENDYMAL TUMORS
74. Chapter 61: Supratentorial Ependymoma
75. Chapter 62: Infratentorial Ependymoma
76. Chapter 63: Embryonal Tumors With Multilayered Rosettes
77. CHOROID PLEXUS TUMORS
78. Chapter 64: Choroid Plexus Papilloma
79. Chapter 65: Choroid Plexus Carcinoma
80. NEURONAL AND MIXED NEURONALGLIAL TUMORS
81. Chapter 66: Ganglioglioma
82. Chapter 67: Desmoplastic Infantile Tumors
83. PINEAL PARENCHYMAL TUMORS
84. Chapter 68: Pineoblastoma
85. EMBRYONAL AND NEUROBLASTIC TUMORS
86. Chapter 69: Medulloblastoma
87. Chapter 70: Atypical Teratoid/Rhabdoid Tumor
88. Chapter 71: Metastatic Neuroblastoma
89. HISTIOCYTIC AND HEMATOPOETIC TUMORS
90. Chapter 72: Leukemia
91. Chapter 73: Langerhans Cell Histiocytosis, Skull and Brain
92. GERM CELL TUMORS
93. Chapter 74: Germinoma
94. Chapter 75: Teratoma
95. NONNEOPLASTIC CYSTS AND TUMOR MIMICS
96. Chapter 76: Arachnoid Cyst
97. Chapter 77: Dermoid Cyst
98. Chapter 78: Epidermoid Cyst
99. Chapter 79: Neuroglial Cyst
100. Chapter 80: Enlarged Perivascular Spaces
101. Chapter 81: Pineal Cyst
102. Chapter 82: Choroid Plexus Cyst
103. Chapter 83: Ependymal Cyst
104. Chapter 84: Porencephalic Cyst
105. Chapter 85: Neurenteric Cyst
106. Chapter 86: Lipoma
107. INFECTIOUS, INFLAMMATORY, AND DEMYELINATING DISEASE: CONGENITAL/NEONATAL INFECTIONS
108. Chapter 87: Congenital CMV
109. Chapter 88: Congenital HIV
110. Chapter 89: Neonatal Herpes Encephalitis
111. Chapter 90: Group B Streptococcal Meningitis
112. Chapter 91: Citrobacter Meningitis
113. ACQUIRED INFECTIONS
114. Chapter 92: Abscess, Brain
115. Chapter 93: Ventriculitis
116. Chapter 94: Empyema
117. Chapter 95: Herpes Encephalitis Type 1
118. Chapter 96: Miscellaneous Encephalitis
119. Chapter 97: Rasmussen Encephalitis
120. Chapter 98: Subacute Sclerosing Panencephalitis
121. Chapter 99: Tuberculosis
122. Chapter 100: Neurocysticercosis
123. Chapter 101: Miscellaneous Parasites
124. INFLAMMATORY AND DEMYELINATING DISEASE
125. Chapter 102: Multiple Sclerosis
126. Chapter 103: ADEM
127. INHERITED METABOLIC/DEGENERATIVE DISORDERS
128. Chapter 104: Approach to Normal Brain Development and Metabolic Disorders
129. NORMAL VARIANTS
130. Chapter 105: Hypomyelination
131. MITOCHONDRIAL DISORDERS
132. Chapter 106: MELAS
133. Chapter 107: Mitochondrial Encephalopathies
134. LYSOSOMAL DISORDERS
135. Chapter 108: Mucopolysaccharidoses
136. Chapter 109: Gangliosidosis (GM2)
137. Chapter 110: Metachromatic Leukodystrophy
138. Chapter 111: Globoid Cell Leukodystrophy
139. PEROXISOMAL DISORDERS
140. Chapter 112: Zellweger Syndrome and Peroxisomal Biogenesis Disorders
141. Chapter 113: X-Linked Adrenoleukodystrophy
142. ORGANIC AND AMINOACIDOPATHIES
143. Chapter 114: Maple Syrup Urine Disease
144. Chapter 115: Urea Cycle Disorders
145. Chapter 116: Glutaric Aciduria Type 1
146. Chapter 117: Canavan Disease
147. Chapter 118: Alexander Disease
148. MISCELLANEOUS
149. Chapter 119: Megalencephaly With Leukoencephalopathy and Cysts
150. Chapter 120: Vanishing White Matter
151. Chapter 121: X-Linked Charcot-Marie-Tooth
152. Chapter 122: PKAN
153. Chapter 123: Huntington Disease
154. Chapter 124: Wilson Disease
155. ACQUIRED TOXIC/METABOLIC/DEGENERATIVE DISORDERS
156. Chapter 125: Hypoglycemia
157. Chapter 126: Kernicterus
158. Chapter 127: Acute Hypertensive Encephalopathy, PRES
159. Chapter 128: Mesial Temporal Sclerosis
160. Chapter 129: Cerebellitis
161. SECTION 2: ANATOMY-BASED DIAGNOSES
162. VENTRICLES AND CISTERNS
163. Chapter 130: Approach to Ventricular Anatomy and Imaging Issues
164. Chapter 131: Cavum Septi Pellucidi
165. Chapter 132: Cavum Velum Interpositum
166. Chapter 133: Benign Enlarged Subarachnoid Spaces
167. Chapter 134: Hydrocephalus
168. Chapter 135: Aqueductal Stenosis
169. Chapter 136: CSF Shunts and Complications
170. SELLA AND PITUITARY
171. Chapter 137: Approach to Pituitary Development
172. Chapter 138: Pituitary Anomalies
173. Chapter 139: Craniopharyngioma
174. Chapter 140: Hypothalamic Hamartoma
175. SKULL, SCALP, AND MENINGES: CONGENITAL
176. Chapter 141: Congenital Calvarial Defects
177. Chapter 142: Craniosynostoses
178. Chapter 143: Cephalocele
179. Chapter 144: Atretic Cephalocele
180. TRAUMA
181. Chapter 145: Calvarial Fracture
182. Chapter 146: Intracranial Hypotension
183. NONNEOPLASTIC AND TUMOR-LIKE DISORDERS
184. Chapter 147: Fibrous Dysplasia
185. Chapter 148: Extramedullary Hematopoiesis
186. Chapter 149: Thick Skull
187. Part II: Head and Neck
188. SECTION 1: TEMPORAL BONE AND SKULL BASE
189. Chapter 150: Classification of Inner Ear Malformations
190. Chapter 151: Labyrinthine Aplasia
191. Chapter 152: Oval Window Atresia
192. Chapter 153: Cochlear Aplasia
193. Chapter 154: Cochlear Hypoplasia
194. Chapter 155: Cochlear Nerve and Cochlear Nerve Canal Aplasia-Hypoplasia
195. Chapter 156: X-Linked Stapes Gusher (DFNX2)
196. Chapter 157: Common Cavity Malformation
197. Chapter 158: Cystic Cochleovestibular Malformation
198. Chapter 159: Large Vestibular Aqueduct
199. Chapter 160: Semicircular Canal Hypoplasia-Aplasia
200. Chapter 161: Endolymphatic Sac Tumor
201. Chapter 162: Dermoid and Epidermoid Cysts
202. Chapter 163: CPA-IAC Arachnoid Cyst
203. Chapter 164: Congenital Cholesteatoma
204. Chapter 165: Acquired Cholesteatoma
205. Chapter 166: Skull Base Chondrosarcoma
206. SECTION 2: ORBIT, NOSE, AND SINUSES
207. Chapter 167: Nasal Glioma
208. Chapter 168: Frontoethmoidal Cephalocele
209. Chapter 169: Nasal Dermal Sinus
210. Chapter 170: Choanal Atresia
211. Chapter 171: Congenital Nasal Pyriform Aperture Stenosis
212. Chapter 172: Juvenile Angiofibroma
213. Chapter 173: Anophthalmia/Microphthalmia
214. Chapter 174: Macrophthalmia
215. Chapter 175: Coloboma
216. Chapter 176: Nasolacrimal Duct Mucocele
217. Chapter 177: Orbital Dermoid and Epidermoid
218. Chapter 178: Orbital Cellulitis
219. Chapter 179: Orbital Vascular Malformations
220. Chapter 180: Orbital Infantile Hemangioma
221. Chapter 181: Retinoblastoma
222. SECTION 3: SUPRAHYOID AND INFRAHYOID NECK
223. Chapter 182: Approach to Congenital Lesions of Neck
224. Chapter 183: Lingual Thyroid
225. Chapter 184: Oral Cavity Dermoid and Epidermoid
226. Chapter 185: Reactive Lymph Nodes
227. Chapter 186: Suppurative Adenitis
228. SECTION 4: MULTIPLE REGIONS, HEAD AND NECK
229. Chapter 187: 1st Branchial Cleft Cyst
230. Chapter 188: 2nd Branchial Cleft Cyst
231. Chapter 189: 3rd Branchial Cleft Cyst
232. Chapter 190: 4th Branchial Cleft Cyst
233. Chapter 191: Thyroglossal Duct Cyst
234. Chapter 192: Cervical Thymic Cyst
235. Chapter 193: Venous Malformation
236. Chapter 194: Lymphatic Malformation, Cervical
237. Chapter 195: Infantile Hemangioma
238. Chapter 196: Neurofibromatosis Type 1, Head and Neck
239. Chapter 197: Brachial Plexus Schwannoma in Perivertebral Space
240. Chapter 198: Fibromatosis Colli
241. Chapter 199: Rhabdomyosarcoma
242. Chapter 200: Melanotic Neuroectodermal Tumors
243. Chapter 201: Orbital Neurofibromatosis Type 1
244. Part III: Spine
245. SECTION 1: CONGENITAL AND GENETIC DISORDERS
246. CONGENITAL: NORMAL ANATOMICAL VARIATIONS
247. Chapter 202: Filum Terminale Fibrolipoma
248. Chapter 203: Ventriculus Terminalis
249. CHIARI DISORDERS
250. Chapter 204: Chiari 1 Malformation
251. Chapter 205: Chiari 2 Malformation
252. Chapter 206: Chiari 3 Malformation
253. ABNORMALITIES OF NEURULATION
254. Chapter 207: Approach to Spine and Spinal Cord Development
255. Chapter 208: Myelomeningocele
256. Chapter 209: Lipomyelomeningocele
257. Chapter 210: Dorsal Dermal Sinus
258. Chapter 211: Dermoid Cyst
259. Chapter 212: Epidermoid Cyst
260. ANOMALIES OF CAUDAL CELL MESS
261. Chapter 213: Tethered Spinal Cord
262. Chapter 214: Segmental Spinal Dysgenesis
263. Chapter 215: Caudal Regression Syndrome
264. Chapter 216: Myelocystocele
265. Chapter 217: Anterior Sacral Meningocele
266. Chapter 218: Sacral Extradural Arachnoid Cyst
267. Chapter 219: Sacrococcygeal Teratoma
268. ANOMALIES OF NOTOCHORD AND VERTEBRAL FORMATION
269. Chapter 220: Craniovertebral Junction Variants
270. Chapter 221: Klippel-Feil Spectrum
271. Chapter 222: Failure of Vertebral Formation
272. Chapter 223: Vertebral Segmentation Failure
273. Chapter 224: Partial Vertebral Duplication
274. Chapter 225: Diastematomyelia
275. Chapter 226: Incomplete Fusion, Posterior Element
276. Chapter 227: Neurenteric Cyst
277. DEVELOPMENTAL ABNORMALITIES
278. Chapter 228: Lateral Meningocele
279. Chapter 229: Dorsal Spinal Meningocele
280. Chapter 230: Dural Dysplasia
281. GENETIC DISORDERS
282. Chapter 231: Neurofibromatosis Type 1
283. Chapter 232: Neurofibromatosis Type 2
284. Chapter 233: Achondroplasia
285. Chapter 234: Mucopolysaccharidoses
286. Chapter 235: Sickle Cell Disease
287. Chapter 236: Osteogenesis Imperfecta
288. SCOLIOSIS AND KYPHOSIS
289. Chapter 237: Developmental Spinal Stenosis
290. Chapter 238: Neuromuscular Scoliosis
291. Chapter 239: Idiopathic Scoliosis
292. Chapter 240: Idiopathic Kyphosis
293. SECTION 2: TRAUMA
294. Chapter 241: Apophyseal Ring Fracture
295. SECTION 3: DEVELOPMENTAL AND DEGENERATIVE DISEASES
296. Chapter 242: Schmorl Node
297. Chapter 243: Scheuermann Disease
298. Chapter 244: Congenital Scoliosis and Kyphosis
299. Chapter 245: Spondylolysis and Spondylolisthesis
300. SECTION 4: INFECTION AND INFLAMMATORY DISORDERS
301. INFECTIONS
302. Chapter 246: Pyogenic Osteomyelitis
303. Chapter 247: Tuberculous Osteomyelitis
304. INFLAMMATORY AND AUTOIMMUNE DISORDERS
305. Chapter 248: Idiopathic Acute Transverse Myelitis
306. Chapter 249: Neuromyelitis Optica
307. Chapter 250: ADEM
308. Chapter 251: Guillain-Barré Syndrome
309. Chapter 252: Acute Flaccid Myelitis
310. SECTION 5: NEOPLASMS, CYSTS, AND OTHER MASSES
311. NEOPLASMS: EXTRADURAL SPACE
312. Chapter 253: Osteoid Osteoma
313. Chapter 254: Osteoblastoma
314. Chapter 255: Aneurysmal Bone Cyst
315. Chapter 256: Osteochondroma
316. Chapter 257: Osteosarcoma
317. Chapter 258: Chordoma
318. Chapter 259: Ewing Sarcoma
319. Chapter 260: Leukemia, Spine
320. Chapter 261: Neuroblastic Tumors
321. Chapter 262: Langerhans Cell Histiocytosis
322. Chapter 263: Angiolipoma
323. INTRADURAL EXTRAMEDULLARY SPACE
324. Chapter 264: Spinal Lipoma
325. Chapter 265: CSF Disseminated Metastases
326. Chapter 266: Myxopapillary Ependymoma
327. INTRAMEDULLARY SPACE
328. Chapter 267: Astrocytoma
329. Chapter 268: Cellular Ependymoma
330. NONNEOPLASTIC CYSTS AND TUMOR MIMICS
331. Chapter 269: Syringomyelia
332. Chapter 270: Epidural Lipomatosis
333. Chapter 271: Extramedullary Hematopoiesis
334. SECTION 6: SPINE POSTPROCEDURAL IMAGING
335. Chapter 272: Hardware Failure

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