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Book ; Online: Letters to Alice

Kleberg, Robert Justus / Kleberg, Alice Gertrudis King / Monday, Jane Clements / Vick, Frances Brannen

birth of the Kleberg-King Ranch dynasty

(Gulf Coast Books, sponsored by Texas A&M University-Corpus Christi)

2012

Abstract: ... On that same journey, the young lawyer also first laid eyes on Alice King, "Princess of the Wild Horse Desert ... letters written by Kleberg to Alice Gertrudis King provide a glimpse of the lives of two of the most ... influential people in Texas history. Editors Jane Clements Monday and Fran ...

Author's details	edited and annotated by Jane Clements Monday and Frances Brannen Vick; with a foreword by Thomas H. Kreneck
Series title	Gulf Coast Books, sponsored by Texas A&M University-Corpus Christi
Abstract	In the summer of 1881, Robert Justus Kleberg rode across the hot, dusty South Texas brush country to the palatial home of Capt. Richard King to consult with the cattle baron about attending to his legal affairs. On that same journey, the young lawyer also first laid eyes on Alice King, "Princess of the Wild Horse Desert." Neither of their lives would ever be the same. Published for the first time in this book, the love letters written by Kleberg to Alice Gertrudis King provide a glimpse of the lives of two of the most influential people in Texas history. Editors Jane Clements Monday and Fran Includes bibliographical references and index Prologue, 1853-1883 -- A desert empire -- Princess of the Wild Horse Desert -- A young lawyer establishes himself -- Tragedy strikes -- A friendship deepens -- The love letters, 1884-1887 -- My dear little heart -- My little darling -- My little pet -- My darling little wife -- Epilogue, 1887-2011 -- The children of Robert and Alice -- The dynasty -- The empire continues
Language	English
Size	Online-Ressource
Edition	1st ed
Publisher	Texas A&M University Press
Publishing place	College Station, Tex
Document type	Book ; Online
Note	Description based upon print version of record
ISBN	1603444718 ; 9781603443319 ; 9781603444712 ; 1603443312
Database	Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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Article ; Online: Alice in Wonderland syndrome: An imitator of psychosis and other medical conditions.

King, Joel / Leow, Fiona / Cabarkapa, Sonja / Ng, Chee

The Australian and New Zealand journal of psychiatry

2018 Volume 52, Issue 8, Page(s) 806–807

MeSH term(s)	Alice in Wonderland Syndrome/diagnosis ; Diagnosis, Differential ; Humans ; Male ; Psychotic Disorders/diagnosis ; Young Adult
Language	English
Publishing date	2018-03-19
Publishing country	England
Document type	Case Reports ; Letter
ZDB-ID	221140-3
ISSN	1440-1614 ; 0004-8674
ISSN (online)	1440-1614
ISSN	0004-8674
DOI	10.1177/0004867418763528
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Zs.A 856: Show issues

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Article ; Online: Parkinson's disease: symptoms and medications at the end of life.

Wilson, Elisabeth Alice / King-Oakley, Emily / Richfield, Edward William

BMJ supportive & palliative care

2024 Volume 13, Issue e3, Page(s) e912–e915

Abstract: Objectives: People with Parkinson's disease (PwP) have a high palliative symptom burden throughout their disease course, equivalent to advanced malignancy. We aim to establish trends in symptom frequency and prescribing in the 72 hours prior to death ... ...

Abstract	Objectives: People with Parkinson's disease (PwP) have a high palliative symptom burden throughout their disease course, equivalent to advanced malignancy. We aim to establish trends in symptom frequency and prescribing in the 72 hours prior to death for PwP. Methods: Retrospective case note review of PwP who died between February 2019 and September 2020. Results: 51 patients were included. 60.78% of patients (n=31) had agitation and 58.82% (n=30) had pain in the final 72 hours. Patients with cognitive impairment were 4.67 times more likely to experience agitation (p=0.035) compared with those without, with higher total midazolam doses (29.18 mg vs 11.4 mg, p=0.21). Terminal motor symptoms were recorded in three patients. 28.57% of patients received the recommended dose of rotigotine for dopaminergic therapy. Conclusions: PwP have a significant symptom burden at the end of life (EOL) with levels of terminal agitation at the higher end of those expected in the general population. There was a trend towards higher doses of sedation, rather than analgesia, in people with coexistent cognitive impairment.Terminal stiffness, despite being seldom documented in the literature, is an important although infrequent symptom.Rotigotine use at EOL remains commonplace and better understanding of its effect and dosing is required.
MeSH term(s)	Humans ; Parkinson Disease/complications ; Parkinson Disease/drug therapy ; Retrospective Studies ; Tetrahydronaphthalenes/adverse effects ; Pain/drug therapy ; Pain/etiology ; Death ; Thiophenes
Chemical Substances	rotigotine (87T4T8BO2E) ; Tetrahydronaphthalenes ; Thiophenes
Language	English
Publishing date	2024-01-08
Publishing country	England
Document type	Journal Article
ISSN	2045-4368
ISSN (online)	2045-4368
DOI	10.1136/spcare-2023-004389
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Mixed messages from the 'Mild Traumatic Brain Injury' and 'Sport-related Concussion' literatures: Clinical implications.

King, Nigel S / Coates, Alice

Brain injury

2021 Volume 35, Issue 4, Page(s) 501–503

Abstract: ... ...

Abstract	Objectives
MeSH term(s)	Anxiety/etiology ; Brain Concussion/etiology ; Cognitive Behavioral Therapy ; Humans ; Post-Concussion Syndrome/diagnosis ; Post-Concussion Syndrome/etiology ; Sports
Language	English
Publishing date	2021-02-26
Publishing country	England
Document type	Journal Article
ZDB-ID	639115-1
ISSN	1362-301X ; 0269-9052
ISSN (online)	1362-301X
ISSN	0269-9052
DOI	10.1080/02699052.2021.1890216
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Article ; Online: Surgical Management of Congenital Lung Malformations.

King, Alice / Olutoye, Oluyinka O / Lee, Timothy C / Keswani, Sundeep G

NeoReviews

2023 Volume 24, Issue 2, Page(s) e84–e96

Abstract: Congenital lung malformations (CLMs) are commonly diagnosed prenatal lesions with varied natural history. Prenatal diagnosis and monitoring help to guide fetal interventions, delivery planning, and need for urgent perinatal surgical interventions. All ... ...

Abstract	Congenital lung malformations (CLMs) are commonly diagnosed prenatal lesions with varied natural history. Prenatal diagnosis and monitoring help to guide fetal interventions, delivery planning, and need for urgent perinatal surgical interventions. All prenatally diagnosed CLMs should be evaluated postnatally, typically with cross-sectional imaging, because many lesions persist despite the appearance of complete 'regression' in utero. Management of CLMs in asymptomatic infants weighs the surgical and anesthetic risk of prophylactic resection against the risk of expectant management, including the possibility of infection, malignant degeneration, and more complicated surgical resection later with loss of compensatory lung growth.
MeSH term(s)	Infant ; Female ; Pregnancy ; Humans ; Prenatal Diagnosis ; Lung/diagnostic imaging ; Lung/surgery
Language	English
Publishing date	2023-01-31
Publishing country	United States
Document type	Journal Article
ISSN	1526-9906
ISSN (online)	1526-9906
DOI	10.1542/neo.24-2-e84
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Article ; Online: Treatment Facility Case Volume and Disparities in Outcomes of Congenital Diaphragmatic Hernia Cases.

Peiffer, Sarah E / Mehl, Steven C / Powell, Paulina / Lee, Timothy C / Keswani, Sundeep G / King, Alice

Journal of pediatric surgery

2024 Volume 59, Issue 5, Page(s) 825–831

Abstract: Introduction: Congenital diaphragmatic hernia (CDH) is a life-threatening, prenatally diagnosed congenital anomaly. We aim to characterize care and outcomes of infants with CDH in Texas and the impact of treating facilities volume of care.: Methods: ... ...

Abstract	Introduction: Congenital diaphragmatic hernia (CDH) is a life-threatening, prenatally diagnosed congenital anomaly. We aim to characterize care and outcomes of infants with CDH in Texas and the impact of treating facilities volume of care. Methods: Retrospective cohort study using a state-wide Hospital Inpatient Discharge Public Use Data File was conducted (2013-2021). Neonates and infants <1 year of age were included using CDH ICD-9/ICD-10 codes. Neonates transferred to an outside hospital were excluded to avoid double-counting. Descriptive statistics, chi-square and logistic regression analysis were performed. Results: Of 1314 CDH patient encounters identified, 728 (55%) occurred at 5 higher volume centers (HVC, >75 cases), 326 (25%) at 9 mid-volume centers (MVC, 20-75 cases) and 268 (20%) at 79 low volume centers (LVC, <20 cases). HVC had lower mortality rates (18%, MVC 22% vs LVC 27%; p = 0.011) despite treating sicker patients (extreme illness severity: HVC 71%, MVC 62% vs LVC 50%; p < 0.001) with longer length-of-stay (p < 0.001). Extracorporeal membrane oxygenation was used in 136 (10%) and provided primarily at HVC. LVC treated proportionately more non-white Hispanic patients (p < 0.001) and patients from counties along the Mexican border (p < 0.001). The predicted probability of mortality in CDH patients decreases with higher treatment facility CDH case volume, with a 0.5% decrease in the odds of mortality for every additional CDH case treated (p < 0.001). Conclusions: Patients treated in HVC have significantly lower mortality despite increased severity. Our data suggest minority populations may be disproportionately treated at LVC associated with worse outcomes. Type of study: Retrospective Prognosis Study. Level of evidence: Level II.
MeSH term(s)	Infant, Newborn ; Infant ; Humans ; Hernias, Diaphragmatic, Congenital/therapy ; Retrospective Studies ; Prognosis ; Probability ; Extracorporeal Membrane Oxygenation
Language	English
Publishing date	2024-02-04
Publishing country	United States
Document type	Journal Article
ZDB-ID	80165-3
ISSN	1531-5037 ; 0022-3468
ISSN (online)	1531-5037
ISSN	0022-3468
DOI	10.1016/j.jpedsurg.2024.01.042
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Article: Patient Satisfaction in Neurosurgery Clinic.

Wang, Alice S / Wiginton, James G / Tran, Theo / Yanez, Paulino / King, Christopher / Miulli, Dan E

Cureus

2024 Volume 16, Issue 1, Page(s) e53176

Abstract: Background: National commercial surveys are used to assess patient satisfaction. However, the information obtained does not always correspond to the clinical situation and therefore may be inadequate to help improve a specific patient experience when ... ...

Abstract	Background: National commercial surveys are used to assess patient satisfaction. However, the information obtained does not always correspond to the clinical situation and therefore may be inadequate to help improve a specific patient experience when through no fault of its design, results in low response rates and inadequate specifics. Objective: The objective is to investigate patient satisfaction using real-time in-person patient experience survey responses at the end of a neurosurgical clinic visit and review the results from these survey responses and those from national commercial survey responses provided by the hospital for the ability to affect change. Methods: This is a prospective study from October 2023 to December 2023 during which a paper copy of 10 questionnaires derived from a national commercial outpatient clinical survey was given to every unique patient who was neurologically capable of filling it out at the end of his or her neurosurgery clinic visit. The electronic medical record was used to collect patient demographics and details of the clinic visit. National commercial survey responses from July 2022 to November 2023 provided by the hospital were reviewed. Results: A total of 149 patients were seen in the neurosurgery clinic from October 2023 to December 2023, 121 patients were given the in-person patient satisfaction survey, and the response rate was 100%. The mean age was 46.5 years with females constituted 45.5% of the patient sample. The visit type included 46 (38.0%) new patients, 53 (43.8%) returning patients, and 22 (18.2%) post-op patients, of which 45.5% presented with cranial pathologies. Comparing the patient satisfaction level between those seen by one provider and those seen by two providers, such as resident, or mid-level with attending, patients seen by two providers were less satisfied with "feeling respected by the providers" (4.92 vs. 4.64, p=0.0088), "feeling listened to by the providers" (4.84 vs. 4.50, p=0.0180), and "feeling appreciated that the providers discussed illness prevention" (4.72 vs. 4.29, p=0.0232). Due to a lack of necessary information from our national commercial outpatient clinic survey responses provided by the hospital, a direct comparison between the in-person survey and our national commercial outpatient clinic survey was not made. Conclusions: Patient satisfaction surveys when not given in real-time in-person run the risk of low response rate and lack of specifics to help guide providers in quality improvement. Our data supports the use of real-time in-person patient satisfaction surveys that not only increase response rate but also provide useful information to help improve patient experience.
Language	English
Publishing date	2024-01-29
Publishing country	United States
Document type	Journal Article
ZDB-ID	2747273-5
ISSN	2168-8184
ISSN	2168-8184
DOI	10.7759/cureus.53176
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Life-Long Steroid Responsive Familial Myopathy With Docking Protein 7 Mutation.

Oh, Shin J / King, Peter H / Schindler, Alice

Journal of clinical neuromuscular disease

2022 Volume 24, Issue 2, Page(s) 80–84

Abstract: Abstract: Docking protein 7 (DOK7) congenital myasthenic syndrome (CMS) is characterized by limb-girdle weakness and lack of fluctuating fatigability simulating many familial myopathies. Albuterol is the first line of therapy in view of consistent ... ...

Abstract	Abstract: Docking protein 7 (DOK7) congenital myasthenic syndrome (CMS) is characterized by limb-girdle weakness and lack of fluctuating fatigability simulating many familial myopathies. Albuterol is the first line of therapy in view of consistent improvement. Two brothers with progressive predominant biceps weakness for 1-3 years responded to prednisone treatment for 40-50 years. Various studies including muscle biopsy and many laboratory studies were unsuccessful for the definite diagnosis. Gene study, 40 years after the initial evaluation, confirmed the diagnosis of DOK7 CMS. These are the first reported cases of DOK7 CMS associated with a sustained benefit from corticosteroids.
MeSH term(s)	Humans ; Male ; Albuterol ; Muscle Weakness ; Mutation/genetics ; Myasthenic Syndromes, Congenital/genetics ; Steroids
Chemical Substances	Albuterol (QF8SVZ843E) ; Steroids ; DOK7 protein, human
Language	English
Publishing date	2022-11-30
Publishing country	United States
Document type	Journal Article
ZDB-ID	1454947-5
ISSN	1537-1611 ; 1522-0443
ISSN (online)	1537-1611
ISSN	1522-0443
DOI	10.1097/CND.0000000000000398
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Article ; Online: Drugs Form Ternary Complexes with Human Liver Fatty Acid Binding Protein (FABP1) and FABP1 Binding Alters Drug Metabolism.

Yabut, King Clyde B / Martynova, Alice / Nath, Abhinav / Zercher, Benjamin P / Bush, Matthew F / Isoherranen, Nina

Molecular pharmacology

2024

Abstract: Liver fatty acid binding protein (FABP1) binds diverse endogenous lipids and is highly expressed in the human liver. Binding to FABP1 alters the metabolism and homeostasis of endogenous lipids in the liver. Drugs have also been shown to bind to rat FABP1, ...

Abstract	Liver fatty acid binding protein (FABP1) binds diverse endogenous lipids and is highly expressed in the human liver. Binding to FABP1 alters the metabolism and homeostasis of endogenous lipids in the liver. Drugs have also been shown to bind to rat FABP1, but limited data is available for human FABP1 (hFABP1). FABP1 has a large binding pocket and up to two fatty acids can bind to FABP1 simultaneously. We hypothesized that drug binding to hFABP1 results in formation of ternary complexes and that FABP1 binding alters drug metabolism. To test these hypotheses, native protein mass spectrometry (MS) and fluorescent 11-(dansylamino)undecanoic acid (DAUDA) displacement assays were used to characterize drug binding to hFABP1, and diclofenac oxidation by cytochrome P450 2C9 (CYP2C9) was studied in the presence and absence of hFABP1. DAUDA binding to hFABP1 involved high (K
Language	English
Publishing date	2024-04-05
Publishing country	United States
Document type	Journal Article
ZDB-ID	124034-1
ISSN	1521-0111 ; 0026-895X
ISSN (online)	1521-0111
ISSN	0026-895X
DOI	10.1124/molpharm.124.000878
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Article: Drugs Form Ternary Complexes with Human Liver Fatty Acid Binding Protein (FABP1) and FABP1 Binding Alters Drug Metabolism.

Yabut, King Clyde B / Martynova, Alice / Nath, Abhinav / Zercher, Benjamin P / Bush, Matthew F / Isoherranen, Nina

bioRxiv : the preprint server for biology

2024

Abstract	Liver fatty acid binding protein (FABP1) binds diverse endogenous lipids and is highly expressed in the human liver. Binding to FABP1 alters the metabolism and homeostasis of endogenous lipids in the liver. Drugs have also been shown to bind to rat FABP1, but limited data is available for human FABP1 (hFABP1). FABP1 has a large binding pocket and multiple fatty acids can bind to FABP1 simultaneously. We hypothesized that drug binding to hFABP1 results in formation of ternary complexes and that FABP1 binding alters drug metabolism. To test these hypotheses native protein mass spectrometry (MS) and fluorescent 11-(dansylamino)undecanoic acid (DAUDA) displacement assays were used to characterize drug binding to hFABP1 and diclofenac oxidation by cytochrome P450 2C9 (CYP2C9) was studied in the presence and absence of hFABP1. DAUDA binding to hFABP1 involved high (K
Language	English
Publishing date	2024-01-19
Publishing country	United States
Document type	Preprint
DOI	10.1101/2024.01.17.576032
Database	MEDical Literature Analysis and Retrieval System OnLINE

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