Results 181 to 190 of about 170,832 (353)

The function of the adrenal medulla [PDF]

The Journal of Physiology, 1932
E. Annau, A. Szent-Györgyi, J. L. Svirbely, St Huszák   +3 more
openaire   +3 more sources

Morphological development of the ovary in the <i>Alectoris chukar</i> at embryonic and pre-pubertal stages. [PDF]

Vet Res Forum
Teymouri M, Kheirabadi M, Nabipour A.
europepmc   +1 more source

Case Report: Hypomyelinating Leukodystrophy Type 20 (HLD20) With Novel CNP Gene Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT This case report describes a child with hypomyelinating leukodystrophy type 20 (HLD20), a rare neurodegenerative disorder characterized by impaired myelin formation. The patient presented with multiple neurodevelopmental abnormalities, including delayed motor milestones, seizures, and abnormal facial features.
Malak Alghamdi, Ghaida Alghamdi, Khalid Hundallah, Dima Jamjoom, Naif Almontashiri, Essa Alharbi, Muhammad Umair, Majid Alfadhel   +7 more
wiley   +1 more source

Experimental study of intravoxel incoherent motion diffusion imaging combined with ultrasound renal resistance index in contrast-induced nephropathy. [PDF]

BMC Nephrol
Chen J, Song X, Wang Z, Wang Z.
europepmc   +1 more source

Transplantation of the Medulla of Bone [PDF]

, 1882
NULL AUTHOR_ID
openalex   +1 more source

Neuroaxonal Dystrophy With Osteopetrosis Associated With a Novel Biallelic Nonsense Homozygous Variant in BORCS5

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Neuroaxonal dystrophy (NAD) with osteopetrosis syndrome (OMIM # 600329) was first reported in a consanguineous Moroccan Jewish family. However, to date, no genetic variant has been linked to this disease. We report on sibs, born to consanguineous Pakistani parents identified prenatally with cerebral ventriculomegaly and agenesis of the corpus ...
Yael Fisher, Orli Greenberg, Patrick Shannon, Andrea Staines, Bobbi McGivern, Melanie Patricia Napier, David Chitayat   +6 more
wiley   +1 more source

Spatial and Temporal Expression Patterns of EDA2R, PCDH9, and TRAF7 in <i>Yotari</i> (<i>Dab1^-/-</i>) Mice: Implicationsfor Understanding CAKUT Pathogenesis. [PDF]

Int J Mol Sci
Komić J, Kelam N, Racetin A, Filipović N, Saraga-Babić M, Ihara D, Katsuyama Y, Vukojević K.   +7 more
europepmc   +1 more source

Unilateral Inferior Medulla Syndrome. Rotatory Nystagmus [PDF]

, 1921
André‐Thomas, J. Jumentié
openalex   +1 more source

Genetics of Response to ECT, TMS, Ketamine and Esketamine

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Treatment‐resistant mood disorders are often managed with intensive interventions that include electroconvulsive therapy (ECT), transcranial magnetic stimulation (TMS), ketamine, and esketamine, but the role of genetics in clinical response to those interventions is yet to be clearly determined.
Clio E. Franklin, Murat Altinay, Kala Bailey, Mahendra T. Bhati, Brent R. Carr, Susan K. Conroy, Khurshid Khurshid, William M. McDonald, Brian J. Mickey, James W. Murrough, Sean M. Nestor, Thomas Nickl‐Jockschat, Irving M. Reti, Gerard Sanacora, Nicholas T. Trapp, Biju Viswanath, Jesse H. Wright, Peter P. Zandi, James B. Potash   +18 more
wiley   +1 more source

Tumor-mimicking sarcoid-like reaction with lymphoid infiltration showing intracranial extension from the left jugular foramen: illustrative case. [PDF]

J Neurosurg Case Lessons
Kim YJ, Nishihara M, Iwahashi H, Yamanishi S, Ashida N, Hosoda K, Nagashima H, Tanaka K, Sasayama T.   +8 more
europepmc   +1 more source