Dysosteosclerosis presents as an “Osteoclast-Poor” form of osteopetrosis: Comprehensive investigation of a 3-year-old girl and literature review

Creatine kinase brain isoenzyme (BB-CK) presence in serum distinguishes osteopetroses among the sclerosing bone disorders

(2010) Michael P. Whyte et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers-Schönberg disease (Chloride Channel 7 Deficiency Osteopetrosis) among the sclerosing bone disorders

(2010) Michael P Whyte et al.   JOURNAL OF BONE AND MINERAL RESEARCH

The Erlenmeyer flask bone deformity in the skeletal dysplasias

(2009) Maha A. Faden et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Camurati–Engelmann disease: imaging, clinical features and differential diagnosis

(2009) Aldona Bartuseviciene et al.   SKELETAL RADIOLOGY

Human Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia due to TNFRSF11A (RANK) Mutations

(2008) Matteo M. Guerrini et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Clinical and radiologic findings in an adult male with dysosteosclerosis

(2008) Edmond G. Lemire et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Infantile Malignant, Autosomal Recessive Osteopetrosis: The Rich and The Poor

(2008) Anna Villa et al.   CALCIFIED TISSUE INTERNATIONAL

Advances in osteoclast biology resulting from the study of osteopetrotic mutations

(2008) T. Segovia-Silvestre et al.   HUMAN GENETICS