Results 61 to 70 of about 1,070 (125)

[Clinical and molecular genetic features of 3 family cases of the central precocious puberty, due to MKRN3 gene defects]. [PDF]

open access: yesProbl Endokrinol (Mosk), 2021
Zubkova NA   +7 more
europepmc   +1 more source

[Clinical and molecular genetic features of cases of isolated hypogonadotropic hypogonadism, associated with defects in GNRHR genes]. [PDF]

open access: yesProbl Endokrinol (Mosk), 2021
Makretskaya NA   +11 more
europepmc   +1 more source

[Endocrine disorders in patients with transfusion-dependent hereditary anemias]. [PDF]

open access: yesProbl Endokrinol (Mosk), 2022
Vitebskaya AV   +3 more
europepmc   +1 more source

[Combination of macro-TSH and macroprolactinemia phenomena in a patient with autoimmune thyroiditis and vitiligo]. [PDF]

open access: yesProbl Endokrinol (Mosk)
Sazonova DV   +6 more
europepmc   +1 more source

[Metastatic pituitary lesion]. [PDF]

open access: yesProbl Endokrinol (Mosk)
Lapshina AM   +8 more
europepmc   +1 more source

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