Disease Introduction - Kocher-Debre-Semelaigne Syndrome, Brachydactyly, Foix-Alajouanine Syndrome, Ectopia, Zymotic Disease (Paperback)


Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 204. Chapters: Fraser syndrome, Enterococcus faecalis, Costochondritis, Volvulus, Membranoproliferative glomerulonephritis, Central cord syndrome, Progressive bulbar palsy, Eosinophilic fasciitis, Klumpke paralysis, Heavy chain disease, Diffuse myelinoclastic sclerosis, Gianotti-Crosti syndrome, Acute aortic syndrome, Hughes-Stovin syndrome, Peroxisomal disorder, Digestive disease, Bronchorrhea, Acute proliferative glomerulonephritis, Ulnar neuropathy, Meningoencephalitis, Periodic fever, aphthous stomatitis, pharyngitis and adenitis, Pyoderma gangrenosum, CHILD syndrome, Bone marrow failure, Acute tubular necrosis, Kimura disease, Exudate, Sezary's disease, Epidermolysis bullosa dystrophica, Oligohydramnios, Trisomy 22, Danon disease, Protein toxicity, Phyllodes tumor, Oligomenorrhea, Intestinal malrotation, Super AIDS, Doege-Potter syndrome, Pitt-Hopkins syndrome, Brachydactyly, Cor triatriatum, Mixed connective tissue disease, Episodic dyscontrol syndrome, Neurogenic bladder, Young Simpson syndrome, Morquio syndrome, Cleidocranial dysostosis, CFP-10, Congenital muscular dystrophy, Laryngomalacia, Plasmacytoma, Caplan's syndrome, Retropharyngeal abscess, Factor XIII deficiency, Carotid-cavernous fistula, Osteochondrodysplasia, Hay-Wells syndrome, Blackleg (disease), Macrocephaly, Abdominal epilepsy, Duodenal atresia, Sticky platelet syndrome, Intestinal parasite, Blue rubber bleb nevus syndrome, Peritoneal mesothelioma, Dysdiadochokinesia, Familial hypocalciuric hypercalcemia, Hereditary neuropathy with liability to pressure palsy, Distal muscular dystrophy, Cervicitis, Cartilage-hair hypoplasia, Paraphrenia, Lipodermatosclerosis, Renovascular hypertension, Somnolence, Breast disease, Scimitar syndrome, Simple partial seizure, XX male syndrome, HIV/AIDS in Europe, Labyrinthine fistula, Middle cerebral artery syndrome, Fibrosis, Yunis-Varon syndrome, Sulfhemoglobinemia, Maroteaux-Lamy syndrome, Inflammatory myopathy, Female genital prolapse, Eagle syndrome, Asplenia with cardiovascular anomalies, Gray baby syndrome, Lagophthalmos, Pulmonary valve stenosis, Polymorphous light eruption, Marburg multiple sclerosis, Guyon's canal syndrome, Schmorl's nodes, Chorioamnionitis, Anti-NMDA receptor encephalitis, Perforated ulcer, Seckel syndrome, Esophagitis, Situs ambiguus, Posterior cerebral artery syndrome, Rickettsiosis, Cutis laxa, Pagophagia, Harry Raymond Eastlack, Lecithin cholesterol acyltransferase deficiency, Barakat syndrome, Melorheostosis, Sialidosis, Lofgren syndrome, Ruptured spleen, Monteggia fracture, Single umbilical artery, Arteriovenous fistula, Infantile hemangioendothelioma, Permanent neonatal diabetes mellitus, Pasma, Unstable angina, Neuropathy, ataxia, and retinitis pigmentosa, Fibromatosis, Epispadias, Hallux rigidus, Cerebrotendineous xanthomatosis, Subacute bacterial endocarditis, White sponge nevus, Congestive hepatopathy, De Barsy syndrome, Polyphagia, Hypervolemia, Preauricular sinus and cyst, Medial medullary syndrome, Branchial cleft cyst, Coronary steal, Osteopoikilosis, Sinoatrial block, Idiopathic postprandial syndrome, Volkmann's contracture, Chylothorax, Biliary colic, Acute retinal necrosis, Fissured tongue, Myocardial stunning, Sneddon's syndrome, Mallet finger, Myelophthisic anemia, Ventricular aneurysm, Vesicovaginal fistula, Kohler disease, True hermaphroditism, Intestinal atresia, Orthopnea, Melkersson-Rosenthal syndrome, Pulmonary hemorrhage, Yush disease, Light chain deposition disease, Granulomatous mastitis, Leukorrhea, Cervical ectropion, Paroxysmal cold hemoglobinuria, Photodermatitis, Amelia (birth defect), Polymorphous low-grade adenocarcinoma, Platinosis, Hereditary diffuse leukoencephalopathy with spheroids, Rapunzel syndrome, Activated protein C resistance, Aortoiliac occlusive disease, Ruzicka Goerz Anton syndrome, ...

R876

Or split into 4x interest-free payments of 25% on orders over R50
Learn more

Discovery Miles8760
Mobicred@R82pm x 12* Mobicred Info
Free Delivery
Delivery AdviceOut of stock

Toggle WishListAdd to wish list
Review this Item

Product Description

Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 204. Chapters: Fraser syndrome, Enterococcus faecalis, Costochondritis, Volvulus, Membranoproliferative glomerulonephritis, Central cord syndrome, Progressive bulbar palsy, Eosinophilic fasciitis, Klumpke paralysis, Heavy chain disease, Diffuse myelinoclastic sclerosis, Gianotti-Crosti syndrome, Acute aortic syndrome, Hughes-Stovin syndrome, Peroxisomal disorder, Digestive disease, Bronchorrhea, Acute proliferative glomerulonephritis, Ulnar neuropathy, Meningoencephalitis, Periodic fever, aphthous stomatitis, pharyngitis and adenitis, Pyoderma gangrenosum, CHILD syndrome, Bone marrow failure, Acute tubular necrosis, Kimura disease, Exudate, Sezary's disease, Epidermolysis bullosa dystrophica, Oligohydramnios, Trisomy 22, Danon disease, Protein toxicity, Phyllodes tumor, Oligomenorrhea, Intestinal malrotation, Super AIDS, Doege-Potter syndrome, Pitt-Hopkins syndrome, Brachydactyly, Cor triatriatum, Mixed connective tissue disease, Episodic dyscontrol syndrome, Neurogenic bladder, Young Simpson syndrome, Morquio syndrome, Cleidocranial dysostosis, CFP-10, Congenital muscular dystrophy, Laryngomalacia, Plasmacytoma, Caplan's syndrome, Retropharyngeal abscess, Factor XIII deficiency, Carotid-cavernous fistula, Osteochondrodysplasia, Hay-Wells syndrome, Blackleg (disease), Macrocephaly, Abdominal epilepsy, Duodenal atresia, Sticky platelet syndrome, Intestinal parasite, Blue rubber bleb nevus syndrome, Peritoneal mesothelioma, Dysdiadochokinesia, Familial hypocalciuric hypercalcemia, Hereditary neuropathy with liability to pressure palsy, Distal muscular dystrophy, Cervicitis, Cartilage-hair hypoplasia, Paraphrenia, Lipodermatosclerosis, Renovascular hypertension, Somnolence, Breast disease, Scimitar syndrome, Simple partial seizure, XX male syndrome, HIV/AIDS in Europe, Labyrinthine fistula, Middle cerebral artery syndrome, Fibrosis, Yunis-Varon syndrome, Sulfhemoglobinemia, Maroteaux-Lamy syndrome, Inflammatory myopathy, Female genital prolapse, Eagle syndrome, Asplenia with cardiovascular anomalies, Gray baby syndrome, Lagophthalmos, Pulmonary valve stenosis, Polymorphous light eruption, Marburg multiple sclerosis, Guyon's canal syndrome, Schmorl's nodes, Chorioamnionitis, Anti-NMDA receptor encephalitis, Perforated ulcer, Seckel syndrome, Esophagitis, Situs ambiguus, Posterior cerebral artery syndrome, Rickettsiosis, Cutis laxa, Pagophagia, Harry Raymond Eastlack, Lecithin cholesterol acyltransferase deficiency, Barakat syndrome, Melorheostosis, Sialidosis, Lofgren syndrome, Ruptured spleen, Monteggia fracture, Single umbilical artery, Arteriovenous fistula, Infantile hemangioendothelioma, Permanent neonatal diabetes mellitus, Pasma, Unstable angina, Neuropathy, ataxia, and retinitis pigmentosa, Fibromatosis, Epispadias, Hallux rigidus, Cerebrotendineous xanthomatosis, Subacute bacterial endocarditis, White sponge nevus, Congestive hepatopathy, De Barsy syndrome, Polyphagia, Hypervolemia, Preauricular sinus and cyst, Medial medullary syndrome, Branchial cleft cyst, Coronary steal, Osteopoikilosis, Sinoatrial block, Idiopathic postprandial syndrome, Volkmann's contracture, Chylothorax, Biliary colic, Acute retinal necrosis, Fissured tongue, Myocardial stunning, Sneddon's syndrome, Mallet finger, Myelophthisic anemia, Ventricular aneurysm, Vesicovaginal fistula, Kohler disease, True hermaphroditism, Intestinal atresia, Orthopnea, Melkersson-Rosenthal syndrome, Pulmonary hemorrhage, Yush disease, Light chain deposition disease, Granulomatous mastitis, Leukorrhea, Cervical ectropion, Paroxysmal cold hemoglobinuria, Photodermatitis, Amelia (birth defect), Polymorphous low-grade adenocarcinoma, Platinosis, Hereditary diffuse leukoencephalopathy with spheroids, Rapunzel syndrome, Activated protein C resistance, Aortoiliac occlusive disease, Ruzicka Goerz Anton syndrome, ...

Customer Reviews

No reviews or ratings yet - be the first to create one!

Product Details

General

Imprint

Books LLC, Wiki Series

Country of origin

United States

Release date

December 2012

Availability

Supplier out of stock. If you add this item to your wish list we will let you know when it becomes available.

First published

December 2012

Authors

Dimensions

246 x 189 x 11mm (L x W x T)

Format

Paperback - Trade

Pages

308

ISBN-13

978-1-233-26365-3

Barcode

9781233263653

Categories

LSN

1-233-26365-X



Trending On Loot