Results 61 to 70 of about 12,963 (181)

Association of the PD‐L1 CPS With the Efficacy of First‐Line Nivolumab Plus Chemotherapy for Unresectable Advanced or Recurrent Gastric Cancer

Cancer Medicine, Volume 15, Issue 7, July 2026.
ABSTRACT Background The CheckMate 649 trial showed the superiority of first‐line nivolumab plus chemotherapy (Nivo‐CT) over chemotherapy alone for advanced gastric or gastroesophageal junction (GEJ) cancer with a programmed cell death‐ligand 1 (PD‐L1) combined positive score (CPS) ≥ 5.
Nozomu Ogura, Misa Ohnishi, Rin Inamoto, Yosuke Kito, Kengo Nagashima, Naoki Takahashi, Mitsuhiro Furuta, Hirokazu Shoji   +7 more
wiley   +1 more source

Clinical Profile of Patients with Hypopituitarism in a Tertiary Care Centre in Central India

Indian Journal of Endocrinology and Metabolism
Introduction: Hypopituitarism is a serious endocrine illness with life-threatening implications. There is a lack of reliable Indian epidemiological data, with very few studies on hypopituitarism across the country.
Vinay R. Pandit, Kritika Pant, Amritava Ghosh, Pankaj K. Kannauje, Jhasaketan Meher   +4 more
doaj   +1 more source

Hypopituitarism after Orthohantavirus Infection: What is Currently Known?

Viruses, 2019
Several case reports have described hypopituitarism following orthohantavirus infection, mostly following Puumala virus. The pathogenesis of this seemingly rare complication of orthohantavirus infection remains unknown.
Soerajja Bhoelan, Thomas Langerak, Danny Noack, Linda van Schinkel, Els van Nood, Eric C.M. van Gorp, Barry Rockx, Marco Goeijenbier   +7 more
doaj   +1 more source

Pituitary dysfunction following traumatic brain injury: clinical perspectives

Neuropsychiatric Disease and Treatment, 2015
Fatih Tanriverdi, Fahrettin Kelestimur Department of Endocrinology, Erciyes University Medical School, Kayseri, Turkey Abstract: Traumatic brain injury (TBI) is a well recognized public health problem worldwide.
Tanriverdi F, Kelestimur F
doaj  

CHOLESTASIS, HYPOGLYCEMIA AND UNUSUAL PHENOTYPE AS THE MANIFESTATIONS OF CONGENITAL HYPOPITUITARISM AS PART OF MONOSOMY 18P- SYNDROME

Медицинский совет, 2018
The monosomy 18p-syndrome refers to an extremely rare disorder (1:50,000 live-born infants). Congenital hypopituitarism is one of the manifestations of this syndrome in 13% of cases. The rarity of this pathology causes difficulties in the early detection
A. V. Degtyareva, A. A. Puchkova, A. V. Bolmasova, M. A. Melikyan   +3 more
doaj   +1 more source

Hypopituitarism Induced by Continuous Infusion of PGI2 Analogues: A Case Series and the Role of ACTH Screening and Hydrocortisone Treatment

Pulmonary Circulation
Hypopituitarism has been reported in patients receiving continuous infusions of prostaglandin I2 (PGI2) analogues for pulmonary hypertension (PH). However, these patients' clinical characteristics, treatment, and prognoses remain unclear.
Taijyu Satoh, Yuichi Tamura, Noriaki Takama, Hiromi Matsubara, Nobuhiro Tanabe, Takumi Inami, Takahiro Hiraide, Kohtaro Abe, Yoshihiro Dohi, Yoshito Ogihara, Takeshi Ogo, Shiro Adachi, Kazuhiko Nakazato, Ichizo Tsujino, Hideki Ota, Kohei Komaru, Haruka Sato, Yuta Tezuka, Yoshikiyo Ono, Rika Suda, Kazuya Hosokawa, Sarasa Isobe, Takatoyo Kiko, Yuki Koga, Junichi Nakamura, Koichiro Sugimura, Masaru Hatano, Yoshihiro Fukumoto, Satoshi Yasuda   +28 more
doaj   +1 more source

Characteristics of NAFLD Based on Hypopituitarism

Canadian Journal of Gastroenterology and Hepatology, 2020
Background. Hypopituitarism and hypothalamic disorders, which induce central obesity and appetite disorder, are associated with nonalcoholic fatty liver disease (NAFLD).
Kazuhisa Kodama, Atsuhiro Ichihara, Yasufumi Seki, Yuichi Ikarashi, Takaomi Sagawa, Tomomi Kogiso, Maiko Taniai, Katsutoshi Tokushige   +7 more
doaj   +1 more source

Spontaneous successful pregnancy in posthypophysectomy hypopituitarism: A rare case report

Journal of Human Reproductive Sciences, 2014
Pregnancy in patients with pan-hypopituitarism following surgery of pituitary adenoma is rare and considered high risk. Hormonal dysfunction in these patients involves more than one axis (gonadotrophic, thyroidal, and adrenal).
Indu Lata
doaj   +1 more source

Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment

JCRPE, 2019
Hypopituitarism is defined as a decreased release of hypophyseal hormones, which may be caused by disease of the pituitary gland disease or hypothalamus. The clinical findings of neonatal hypopituitarism depend on the causes and on presence and extent of
Selim Kurtoğlu, Ahmet Özdemir, Nihal Hatipoğlu   +2 more
doaj   +1 more source

A Histologically Diagnosed Case with Infantile Osteopetrosis Complicated by Hypopituitarism

Case Reports in Pathology, 2015
Malignant infantile osteopetrosis is a rarely seen severe disorder which appears early in life with general sclerosis of the skeleton. It is caused by functionally defective osteoclasts which fail to resorb bone.
Gulden Diniz, Ozgur Olukman, Sebnem Calkavur, Muammer Buyukinan, Canan Altay   +4 more
doaj   +1 more source