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371 results on '"Haggard M"'

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201. Immunohemolytic anemia and Hodgkin disease.

202. Genetic haemoglobin abnormalities in about 9000 Black and 7000 White newborns; haemoglobin F Dickinson (Agamma97His-Arg), a new variant.

207. Factors influencing survival in pediatric acute leukemia. The SWCCSG experience, 1958-1970.

213. BONE MARROW MORPHOLOGY STUDY.

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.

225. Vincristine in acute leukemia of childhood.

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.

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.

238. Megaloblastic anemia and orotic aciduria. A hereditary disorder of pyrimidine metabolism responsive to uridine.

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.

247. Leukemia in childhood.

248. Infantile genetic agranulocytosis: two cases occurring in siblings and one in a distant relative.

250. HEMOGLOBIN G-COUSHATTA: A NEW VARIANT IN AN AMERICAN INDIAN FAMILY.

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