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「"Machaczka M "[Author]」の検索結果

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Endocrine and metabolic disorders in patients with Gaucher disease type 1: a review.

Polyneuropathy in Gaucher disease type 1 and 3 - a descriptive case series.

Bone and hormonal status 10 years post allogeneic bone marrow transplantation.

First Clinicogenetic Description of Parkinson's Disease Related to Mutation S107L.

Presenting signs and patient co-variables in Gaucher disease: outcome of the Gaucher Early Diagnosis Consensus (GED-C) Delphi initiative.

Hodgkin lymphoma of the elderly patients: a retrospective multicenter analysis from the Polish Lymphoma Research Group.

The influence of various therapeutic regimens on early clinical and laboratory response and outcome of children with secondary hemophagocytic lymphohistiocytosis.

Clinical characteristics, therapy response, and outcome of 51 adult patients with hematological malignancy-associated hemophagocytic lymphohistiocytosis: a single institution experience.

Baseline Characteristics Predicting Very Good Outcome of Allogeneic Hematopoietic Cell Transplantation in Young Patients With High Cytogenetic Risk Chronic Lymphocytic Leukemia - A Retrospective Analysis From the Chronic Malignancies Working Party of the EBMT.

Saccadic Impairments in Patients with the Norrbottnian Form of Gaucher's Disease Type 3.

Centre characteristics and procedure-related factors have an impact on outcomes of allogeneic transplantation for patients with CLL: a retrospective analysis from the European Society for Blood and Marrow Transplantation (EBMT).

Management goals for type 1 Gaucher disease: An expert consensus document from the European working group on Gaucher disease.

Risk factors for treatment failure after allogeneic transplantation of patients with CLL: a report from the European Society for Blood and Marrow Transplantation.

G-CSF mobilized peripheral blood stem cell collection for allogeneic transplantation in healthy donors: Analysis of factors affecting yield.

Aberrant bone marrow vascularization patterns in untreated patients with Gaucher disease type 1.

Ferritinemia and serum inflammatory cytokines in Swedish adults with Gaucher disease type 1.

Novel hyperkinetic dystonia-like manifestation and neurological disease course of Swedish Gaucher patients.

Genetic heterogeneity in primary and relapsed mantle cell lymphomas: Impact of recurrent CARD11 mutations.

The appearance of newly identified intraocular lesions in Gaucher disease type 3 despite long-term glucocerebrosidase replacement therapy.

Atypical cytomorphology of Gaucher cells is frequently seen in bone marrow smears from untreated patients with Gaucher disease type 1.

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