P. Konrad

发表

II. Nonspherocytic Hemolytic Anemia, High Red Cell ATP, and Ribosephosphate Pvrophosphokinase (RPK, E.C. 2.7.6.1) Deficiency

W. Valentine, H. M. Anderson, D. Paglia, 2017 .

Studies on human erythrocyte nucleotide metabolism. II. Nonspherocytic hemolytic anemia, high red cell ATP, and ribosephosphate pyrophosphokinase (RPK, E.C.2.7.6.1) deficiency.

W. Valentine, H. M. Anderson, D. Paglia, 1972, Blood.

Allogeneic bone marrow transplantation for high-risk acute lymphoblastic leukemia during first complete remission.

A. Nademanee, M. Amylon, R. Hoppe, 1991, Blood.

Allogeneic bone marrow transplantation for high-risk acute lymphoblastic leukemia during first complete remission

A. Nademanee, M. Amylon, N. Chao, 1991 .

-Glutamyl-cysteine synthetase deficiency. A cause of hereditary hemolytic anemia.

W. Valentine, D. Paglia, P. Konrad, 1972, The New England journal of medicine.

Pediatric surgical oncology: update on Wilms' tumor, neuroblastoma and rhabdomyosarcoma.

P. Konrad, A. Shaw, 1984, Current problems in cancer.

The distribution of HL-A histocompatibility factors and genes in patients with systemic lupus erythematosus.

R. Walford, P. Konrad, H. Waters, 2008, Tissue antigens.

Allogeneic bone marrow transplantation as therapy for primary induction failure for patients with acute leukemia.

J. Niland, M. Amylon, N. Chao, 1991, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Cytogenetic studies on bone marrow fibroblasts from a male-female hematopoietic chimera. Evidence that stromal elements in human transplantation recipients are of host type.

P. Konrad, B. Greenberg, F. Wilson, 1978, Transplantation.

Erythrocyte Enzymatic Abnormalities in HEMPAS (Hereditary Erythroblastic Multinuclearity with a Positive Acidified‐Serum Test)

W. Valentine, D. Paglia, P. Konrad, 1972, British journal of haematology.

Dyserythropoiesis, refractory anemia, and "preleukemia:" metabolic features of the erythrocytes.

W. Valentine, D. Paglia, P. Konrad, 1973, Blood.

Erythrocyte glyoxalase II deficiency with coincidental hereditary elliptocytosis.

W. Valentine, D. Paglia, P. Konrad, 1970, Blood.

Nonspherocytic Haemolytic Anaemia with Increased Red Cell Adenine Nucleotides, Glutathione and Basophilic Stippling and Ribosephosphate Pyrophosphokinase (RPK) Deficiency: Studies on Two New Kindreds

J. Bennett, W. Krivit, W. Valentine, 1973, British journal of haematology.

Erythrocyte and leukocyte phosphoglycerate kinase deficiency with neurologic disease.

A. Mauer, W. Valentine, D. Paglia, 1973, The Journal of pediatrics.

Acute Childhood Leukaemia in Relation to the HL–A Human Transplantation Genes

R. Walford, P. Konrad, R. Neerhout, 1970, Nature.

Dyserythropoiesis , Refractory Anemia , and “ Preleukemia

W. Valentine, D. Paglia, P. Konrad, 2005 .

Late death fromneuroblastoma

P. Konrad, R. Neerhout, L. J. Singher, 1973 .

Metastasis of adenocarcinoma of the lung to optic nerve sheath meningioma.

R. Lufkin, H. Vinters, Y. Anzai, 1995, Archives of ophthalmology.

An isozyme of erythrocyte pyruvate kinase (PK-Los Angeles) with impaired kinetics corrected by fructose-1, 6-diphosphate.

W. Valentine, D. Paglia, P. Konrad, 1977, American journal of clinical pathology.

Enzymatic activities and glutathione content of erythrocytes in the newborn: comparison with red cells of older normal subjects and those with comparable reticulocytosis.

W. Valentine, D. Paglia, P. Konrad, 1972, Acta haematologica.

Unique phenotypic expression of glucosephosphate isomerase deficiency.

W. Valentine, D. Paglia, P. Konrad, 1975, American journal of human genetics.