371 results on '"Haggard M"'
Search Results
202. Genetic haemoglobin abnormalities in about 9000 Black and 7000 White newborns; haemoglobin F Dickinson (Agamma97His-Arg), a new variant.
203. Population studies into hearing disorders. Implications for general practice.
204. The development of hearing aids for the UK in a European context--role of the public and private sectors.
205. INFLUENCE OF DIET ON BLOOD SERUM LIPIDS IN PREGNANT WOMEN AND NEWBORN INFANTS.
206. Sickling, a quantitatively delayed genetic character.
207. Factors influencing survival in pediatric acute leukemia. The SWCCSG experience, 1958-1970.
208. Perception and production: some correlations on voicing of an initial stop.
209. Haemoglobin P (the Galveston type).
210. AN INHOMOGENEOUS FOETAL HAEMOGLOBIN VARIANT (THE TEXAS TYPE).
211. Stimulus and task factors as determinants of ear advantages.
212. The use of steroids as pharmacologic agents in diseases of children. I. Hematologic disorders.
213. BONE MARROW MORPHOLOGY STUDY.
214. Hypoplastic anemia associated with chloramphenicol therapy.
215. Pitch as a voicing cue.
216. CYCLOPHOSPHAMIDE (NSC-26271)-1 IN UNCOMMON MALIGNANT NEOPLASMS IN CHILDREN.
217. Evaluation of uracil mustard in children with Hodgkin's disease, lymphosarcoma, and soft tissue sarcoma.
218. Remission maintenance therapy for meningeal leukemia: intrathecal methotrexate vs. intravenous bis-nitrosourea.
219. Vincristine sulfate and radiation therapy in metastatic Wilms' tumor.
220. A study of vitamin B 12 requirements in a patient with pernicious anemia and thyrotoxicosis: evidence of an increased need for vitamin B 12 in the presence of hyperthyroidism.
221. Bone infarcts in sickle-cell anemia.
222. Encoding and the REA for speech signals.
223. Staphylococcal pneumonia and empyema in infants in children.
224. Studies of ACTH hydrocortisone, and 6-mercaptopurine in the treatment of children with acute leukemia.
225. Vincristine in acute leukemia of childhood.
226. Development of pediatrics at the University of Texas School of Medicine in Galveston.
227. A new haemoglobin variant exhibiting anomalous electrophoretic behaviour.
228. Selectivity for distortions and words in speech perception.
229. Feasibility of rapid critical bandwidth estimates.
230. Thymic alymphoplasia, lymphoma, and dys-gamma-globulinemia, hyper-gamma A-, normo-gamma M-, hypo-gamma G, a-gamma D-, and gamma E-globulinemia, plasmacytosis, normal delayed hypersensitivity, severe allergic reactions, and Coombs' positive anemia.
231. A family with hemoglobin G.
232. THE RESPONSE OF ACUTE CHILDHOOD LEUKEMIA TO AN INITIAL AND A SECOND COURSE OF PREDNISONE.
233. Lung changes and chemotherapeutic agents in childhood. Report of a case associated with cyclophosphamide therapy.
234. THE COEXISTENCE OF SICKLE CELL DISEASE AND CONGENITAL HEART DISEASE: A REPORT OF THREE CASES, WITH REPAIR UNDER CARDIOPULMONARY BY-PASS IN TWO.
235. Essential fatty acids in infant nutrition. III. Clinical manifestations of linoleic acid deficiency.
236. Speech waveform measurements in multiple sclerosis.
237. The use of steroids as pharmacologic agents in diseases of children. 2. Hypersensitivity states.
238. Megaloblastic anemia and orotic aciduria. A hereditary disorder of pyrimidine metabolism responsive to uridine.
239. Vincristine (NSC-67574) therapy for acute leukemia in children.
240. L-sarcolysin (NSC-8806) therapy for acute leukemia in children.
241. A new haemoglobin variant in an American Negro.
242. CYTOGENETIC STUDIES. DIAGNOSTIC TOOL IN CLINICAL MEDICINE.
243. Perceptual factors in articulatory defects.
244. Therapy of histiocytosis X with vincristine, vinblastine, and cyclophosphamide. The Southwest Cancer Chemotherapy Study Group.
245. Folic acid, pregnancy, and abruptio placentae.
246. Giant vascular tumors and thrombocytopenia.
247. Leukemia in childhood.
248. Infantile genetic agranulocytosis: two cases occurring in siblings and one in a distant relative.
249. Selectivity versus summation in multiple observation tasks: evidence with spectrum parameter noise in speech.
250. HEMOGLOBIN G-COUSHATTA: A NEW VARIANT IN AN AMERICAN INDIAN FAMILY.
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