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Romosozumab for the treatment of osteoporosis. [electronic resource]

By:

Bandeira, Leonardo

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Producer: 20170719Description: 255-263 p. digitalISSN:

1744-7682

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Available from publisher's website

In: Expert opinion on biological therapy vol. 17

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Publication Type: Journal Article; Review

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1 [The frequency of hemoglobinopathies: the results of nine years of observations].
by Boreux, G
2 [Osteodysplasic geroderma of sex-linked heredity, a new clinical and genetic entity].
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3 [Genetic and hematologic study of a family presenting the Pelger-Huet anomaly associated, in one case, with epilepsy and, in another case, with polythelia].
by Boreux, G
4 [The genetic questionnaire].
by Klein, D
5 [Retinopathy in the course of a homozygous haemoglobinopathy (author's transl)].
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6 [Genetic and hematological study of a family from Ghana suffering from hereditary persistence of fetal hemoglobin associated with beta-thalassemia and hemoglobinosis S].
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7 [Hemoglobin types among 100 persons from Haiti studying in Switzerland and neighboring countries].
by Rabeau-Talleyrand, M T
8 [Long-term psychopathological study of a recidivist delinquent presenting the XYY syndrome].
by Mutrux, S
9 [The detection of beta-thalassemia minor (author's transl)].
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10 [Hematological and genetic investigations of a family affected with May-Hegglin anomaly].
by Boreux, G
11 [Quantitative Coombs' test in autoimmune hemolytic anemia].
by Bally, E
12 [48,XXXY constitution in a 7-month-old infant, whose father has chromosome breaks].
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13 [Two cases of Klinefelter's syndrome with mosaicism (46,XY-47,XXY), one of which is associated with protanopia and the other with unilateral corneal opacities].
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14 [Radiographic findings in geroderma osteodysplastica hereditaria].
by Brocher, J E
15 Hereditary myeloperoxidase deficiency.
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16 Hereditary myeloperoxidase deficiency.
by Cech, P
17 [Haemoglobinosis C/beta-thalassemia double heterozygosity in an Algerian patient with total suppression of haemoglobin A synthesis (author's transl)].
by Boreux, G
18 [A sex-linked disorder: hereditary osteodysplastic geroderma (20 years of observation)].
by Klein, D
19 [Hemoglobin D Punjab. Apropos of 2 families].
by Brügger, E
20 [Chronic myelo-monocytic leukemia in the adult. A propos of 12 cases].
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