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Allgrove, Jeremy
33  results:
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1

GNAQ/GNA11 Mosaicism Is Associated with Abnormal Serum Calc..:

Knöpfel, Nicole ; Zecchin, Davide ; Richardson, Hanna...
Journal of Investigative Dermatology.  144 (2024)  4 - p. 820-832.e9 , 2024
Link: https://doi.org/10.1016/..
 
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2

The European registry for rare bone and mineral conditions ..:

Zurita, Ana Luisa Priego ; Danila, Oana O. ; Allgrove, Jeremy...
Bone Reports.  16 (2022)  - p. 101297 , 2022
Link: https://doi.org/10.1016/..
 
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3

Endocrine Diseases of Newborn: Epidemiology, Pathogenesis, ..:

Taylor-Miller, Tashunka ; Allgrove, Jeremy
Frontiers in Pediatrics.  9 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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4

Genetic Analysis of Pediatric Primary Adrenal Insufficiency..:

Buonocore, Federica ; Maharaj, Avinaash ; Qamar, Younus...
Journal of the Endocrine Society.  5 (2021)  8 - p. , 2021
Link: https://doi.org/10.1210/..
 
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5

Juvenile Paget's disease with compound heterozygous mutatio..:

Naot, Dorit ; Wilson, Louise C. ; Allgrove, Jeremy...
Bone.  130 (2020)  - p. 115098 , 2020
Link: https://doi.org/10.1016/..
 
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6

A New Multisystem Disorder Caused by the Gαs Mutation p.F37..:

Biebermann, Heike ; Kleinau, Gunnar ; Schnabel, Dirk...
The Journal of Clinical Endocrinology & Metabolism.  104 (2018)  4 - p. 1079-1089 , 2018
Link: https://doi.org/10.1210/..
 
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7

Use of insulin pump therapy in children and adolescents wit..:

for the T1D Exchange Clinic Network, the DPV Initiative, and the National Paediatric Diabetes Audit and the Royal College of Paediatrics and Child Health registries ; Sherr, Jennifer L. ; Hermann, Julia M....
Diabetologia.  59 (2015)  1 - p. 87-91 , 2015
Link: https://doi.org/10.1007/..
 
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8

Towards a safety net for management of 22q11.2 deletion syn..:

Habel, Alex ; Herriot, Richard ; Kumararatne, Dinakantha...
European Journal of Pediatrics.  173 (2014)  6 - p. 757-765 , 2014
Link: https://doi.org/10.1007/..
 
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9

Mutational Analysis of the Adaptor Protein 2 Sigma Subunit ..:

Rogers, Angela ; Nesbit, M. Andrew ; Hannan, Fadil M....
The Journal of Clinical Endocrinology & Metabolism.  99 (2014)  7 - p. E1300-E1305 , 2014
Link: https://doi.org/10.1210/..
 
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10

A family with Camurati-Engelman disease. The role of the mi..:

Toumba, Meropi ; Neocleous, Vassos ; Shammas, Christos...
Journal of Pediatric Endocrinology and Metabolism.  26 (2013)  9-10 - p. , 2013
Link: https://doi.org/10.1515/..
 
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11

A family with Camurati-Engelman disease: the role of the mi..:

Toumba, Meropi ; Neocleous, Vassos ; Shammas, Christos...
Journal of Pediatric Endocrinology and Metabolism.  26 (2013)  11-12 - p. , 2013
Link: https://doi.org/10.1515/..
 
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12

Metabolic bone disease:

Allgrove, Jeremy
Paediatrics and Child Health.  21 (2011)  4 - p. 187-193 , 2011
Link: https://doi.org/10.1016/..
 
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13

A MissenseGlial Cells Missing Homolog B(GCMB) Mutation, Asn..:

Mirczuk, Samantha M. ; Bowl, Michael R. ; Nesbit, M. Andrew...
The Journal of Clinical Endocrinology & Metabolism.  95 (2010)  7 - p. 3512-3516 , 2010
Link: https://doi.org/10.1210/..
 
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14

The Parathyroid and Disorders of Calcium and Bone Metabolis:

, In: Brook's Clinical Pediatric Endocrinology,
Allgrove, Jeremy - p. 374-427 , 2010
Link: https://doi.org/10.1002/..
 
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15

Growth and Pubertal Delay in Patients with Epidermolysis Bu..:

Martinez, Anna E. ; Allgrove, Jeremy ; Brain, Caroline
Dermatologic Clinics.  28 (2010)  2 - p. 357-359 , 2010
Link: https://doi.org/10.1016/..
 
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