Pet-Specific Care for the Veterinary Team. Группа авторов

Pet-Specific Care for the Veterinary Team - Группа авторов


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Chondrodystrophy and intervertebral Disc Disease Ciliary Dyskinesia Cleft Lip with Syndactyly Cleft Lip/Palate Cobalamin Malabsorption Collie Eye Anomaly/Choroidal Hypoplasia Color Dilution Alopecia Complement 3 (C3) deficiency Cone Degeneration Cone‐Rod Dystrophy (1, 2, 3, 4, SWD) Congenital Hypothyroidism with Goiter Congenital Keratoconjunctivities Sicca and Ichthyosiform Dermatosis Congenital Macrothrombocytopenia Congenital Myasthenic Syndrome Congenital Stationary Night Blindness Copper Toxicosis Craniomandibular Osteopathy Curly Coat Dry Eye Syndrome Cyclic Hematopoiesis Cyclic Neutropenia Cystic renal Dysplasia and Hepatic Fibrosis Cystinuria (Types I‐A, II‐A, II‐B) Dandy–Walker Malformation Day Blindess Deafness and Vestibular Syndrome Degenerative Myelopathy Dental Hypomineralization Dermatomyositis Dystrophic Epidermolysis Bullosa Early Adult Onset Deafness Early Onset Progressive Polyneuropathy Ectodermal Dysplasia Elliptocytosis Encephalopathy Epidermolysis Bullosa Simplex Epidermolytic Hyperkeratosis Epilepsy (variants) Episodic Falling Syndrome Exercise‐Induced Collapse Exercise‐Induced Metabolic Myopathy Factor IX Deficiency (Hemophilia B) Factor VII Deficiency Factor VIII Deficiency (Hemophilia A) Factor XI Deficiency Factor XII Deficiency Familial Congenital Methemoglobinemia Familial Juvenile Epilepsy Familial Nephropathy Fanconi Syndrome Fucosidosis Gall Bladder Mucocele Formation Gangliosidosis (GM1 & GM2) Generalized Myoclonic Epilepsy Glanzmann's Thrombasthenia Glaucoma Globoid Cell Leukodystrophy/Krabbe’s Disease Glomerulopathy KIRREL2 Glycogen Storage Disease IA, II, III, IIIA Goniodysgenesis and Glaucoma Hereditary Ataxia Hereditary Cataracts Hereditary Deafness (PTPRQ) Hereditary Footpad Hyperkeratosis Hereditary Nasal Parakeratosis Hereditary Nephropathy Hereditary Nephropathy (Alport Syndrome) Hip Dysplasia (markers) Histiocytic Sarcoma (marker) Hyperekplexia (Startle Disease) Hyperoxaluria Hyperuricosuria Hypoadrenocorticism Hypocatalasia Hypokalemic Polymyopathy Hypomyelination and Tremors Ichthyosis Inflammatory Myopathy Inherited Myopathy Iron‐Deficiency Anemia Juvenile Encephalopathy Juvenile Epilepsy Juvenile Laryngeal Paralysis and Polyneuropathy Juvenile Myoclonic Epilepsy Juvenile Onset Polyneuropathy L2‐ Hydroxyglutaric Aciduria Lagotto Storage Disease Laryngeal Paralysis Lethal Acrodermatitis MKLN1 Leukoencephalomyelopathy Ligneous Membranitis Lipoprotein Lipase Deficiency Long QT Syndrome Lundehund Syndrome Lupoid Dermatosis Macrothrombocytopenia Macular Corneal Dystrophy Malignant Hyperthermia Mannosidosis May–Hegglin Anomaly Microphthalmia, Anophthalmia, and Coloboma Mucolipidosis II Mucopolysaccharidosis (I, IIIa, VI, VII, VIII) Mullerian Duct Syndrome
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