Suchergebnisse - "Akinci, B."

PubPharm (48)

1

NIVOLUMAB ASSOCIATED ENDOCRINE ABNORMALITIES : CHALLENGING CASES FROM A REFERENCE CLINIC

enthalten in: Acta endocrinologica (Bucharest, Romania : 2005) | 2022

von Unal, M. | Semiz, G. | Ozdoğan, O. | +5

2

Risk factors for diabetic foot ulcers in metreleptin naïve patients with lipodystrophy

enthalten in: Clinical diabetes and endocrinology | 2021

von Saydam, O. | Ozgen Saydam, B. | Adiyaman, S. | +12

3

Risk factors for diabetic foot ulcers in metreleptin naïve patients with lipodystrophy

enthalten in: Clinical diabetes and endocrinology | 2021

von Saydam, O. | Ozgen Saydam, B. | Adiyaman, S. | +12

4

An update on dapagliflozin for the treatment of heart failure

enthalten in: Drugs of today (Barcelona, Spain : 1998) | 2021

von Akinci, B.

5

An update on dapagliflozin for the treatment of heart failure

enthalten in: Drugs of today | 2021

von Akinci, B.

6

An overview of lipodystrophy and the role of the complement system

enthalten in: Molecular immunology | 2019

von Corvillo, F. | Akinci, B.

7

AN UNUSUAL CASE OF ACQUIRED PARTIAL LIPODYSTROPHY PRESENTING WITH ACANTHOSIS NIGRICANS

enthalten in: Acta endocrinologica (Bucharest, Romania : 2005) | 2019

von Ozdemir Kutbay, N. | Sarer Yurekli, B. | Yasar, Z. | +1

8

MEAN PLATELET VOLUME AND PLATELET FUNCTION ANALYSIS IN ACROMEGALIC PATIENTS BEFORE AND AFTER TREATMENT

enthalten in: Acta endocrinologica (Bucharest, Romania : 2005) | 2016

von Demirpence, M. | Yasar, H. | Colak, A. | +4

9

Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L : a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations

enthalten in: Diabetic medicine : a journal of the British Diabetic Association | 2016

von Demir, T. | Onay, H. | Savage, D. | +8

10

Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor ‐γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations

enthalten in: Diabetic medicine | 2016

von Demir, T. | Onay, H. | Savage, D. | +8

1
2
3
4
5
Nächster »
[5]