Pages that link to "Q46478580"

The following pages link to A single-center experience in 20 patients with infantile malignant osteopetrosis (Q46478580):

Displaying 30 items.

• Role of Ostm1 Cytosolic Complex with Kinesin 5B in Intracellular Dispersion and Trafficking. (Q27320758) (← links)
• Optic nerve compression and retinal degeneration in Tcirg1 mutant mice lacking the vacuolar-type H-ATPase a3 subunit (Q27321701) (← links)
• Transplantation immunology: solid organ and bone marrow (Q33803804) (← links)
• An infant with splenohepatomegaly: a rare cause (Q34210979) (← links)
• Complications of anesthesia for children with malignant infantile osteopetrosis before and after hematopoietic stem cell transplantation (Q34296195) (← links)
• SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity (Q34320437) (← links)
• Rho GTPase expression in human myeloid cells (Q34390890) (← links)
• As little as needed: the extraordinary case of a mild recessive osteopetrosis owing to a novel splicing hypomorphic mutation in the TCIRG1 gene. (Q34643815) (← links)
• RANK-dependent autosomal recessive osteopetrosis: characterization of five new cases with novel mutations (Q35837418) (← links)
• A Histologically Diagnosed Case with Infantile Osteopetrosis Complicated by Hypopituitarism (Q36241404) (← links)
• RANKL cytokine: from pioneer of the osteoimmunology era to cure for a rare disease (Q36898545) (← links)
• Malignant infantile osteopetrosis (Q37043697) (← links)
• Can acetazolamide be used to treat diseases involving increased bone mineral density? (Q37425297) (← links)
• Infantile Osteopetrosis and Juvenile Xanthogranuloma Presenting Together in a Newborn: A Case Report and Literature Review (Q37807411) (← links)
• Hypercalcemia and altered biochemical bone markers in post-bone marrow transplantation osteopetrosis: a case report and literature review (Q37842728) (← links)
• Osteopetrosis: genetics, treatment and new insights into osteoclast function. (Q38123371) (← links)
• Severe neurodegeneration with impaired autophagy mechanism triggered by ostm1 deficiency. (Q39661818) (← links)
• Autosomal recessive osteopetrosis: report of 41 novel mutations in the TCIRG1 gene and diagnostic implications. (Q39666141) (← links)
• Improved Outcomes of Hematopoietic Stem Cell Transplantation in Patients With Infantile Malignant Osteopetrosis Using Fludarabine-Based Conditioning. (Q41199377) (← links)
• Anesthesia Management of a Child with Osteopetrosis (Q41259753) (← links)
• Non-total body irradiation myeloablative conditioning with intravenous busulfan and cyclophosphamide in hematopoietic stem cell transplantation for malignant infantile osteopetrosis. (Q41329564) (← links)
• Diagnostic dilemma: osteopetrosis with superimposed rickets causing neonatal hypocalcemia (Q47746410) (← links)
• A founder mutation in the TCIRG1 gene causes osteopetrosis in the Ashkenazi Jewish population (Q48294281) (← links)
• Synonymous Mutations Add a Layer of Complexity in the Diagnosis of Human Osteopetrosis. (Q51610280) (← links)
• Buried in the Middle but Guilty: Intronic Mutations in the TCIRG1 Gene Cause Human Autosomal Recessive Osteopetrosis. (Q53226516) (← links)
• Osteopetrosis rescue upon RANKL administration to Rankl(-/-) mice: a new therapy for human RANKL-dependent ARO. (Q55056509) (← links)
• Partial depletion of TCR alpha/beta(+)/ CD19(+) cells in matched unrelated transplantation of three patients with osteopetrosis (Q86135950) (← links)
• Identification of novel mutation in autosomal recessive infantile malignant osteopetrosis (Q86486549) (← links)
• Hematopoietic cell transplantation for a child with OSTM1 osteopetrosis (Q89777839) (← links)
• A Rare Case of Malignant Infantile Osteopetrosis Presenting as Frontal Lobe Hemorrhage (Q98613481) (← links)