Results 111 to 120 of about 268 (187)

[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

[Cockayne syndrome: peculiarities of clinical manifestations and algorithm of observation in childhood]. [PDF]

open access: yesProbl Endokrinol (Mosk)
Kungurtseva AL   +6 more
europepmc   +1 more source

Саплементация как новая возможность менеджмента климактерия

open access: yes
Objective. To study the possibility of using supplementation in management of patients suffering from climacteric disorders and having a risk of asthenia and depressive disorders. Patients and methods. The study included 70 menopausal female patients who
Радзинский В.Е.   +5 more
core  

[Metastatic pituitary lesion]. [PDF]

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

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